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HELDIANA 



Botany 

NEW SERIES, NO. 43 



El Nino in Peru: 

Biology and Culture Over 10,000 Years 

Jonathan Haas and Michael O. Dillon, Editors 



July 31, 2003 
Publication 1524 



PUBLISHED BY FIELD MUSEUM OF NATURAL HISTORY 



EL NINO IN PERU: 

BIOLOGY AND CULTURE 

OVER 10,000 YEARS 




Papers from the VIII Annual 

A. WATSON ARMOUR III SPRING SYMPOSIUM 
MAY 28-29, 1 999 CHICAGO 



FIELDIANA 



Botany 

NEW SERIES, NO 43 NATURAL \ F5TC&Y SURVEY 

AUG 8 2003 
LIB&AIN 

El Nino in Peru: 

Biology and Culture Over 10,000 Years 

Jonathan Haas and Michael O. Dillon, Editors 



Field Museum of Natural History 
1400 South Lake Shore Drive 
Chicago, Illinois 60605-2496 
U.S. A. 



Published July 31, 2003 
Publication 1524 



PUBLISHED BY FIELD MUSEUM OF NATURAL HISTORY 



2003 Field Museum of Natural History 

ISSN 0015-0746 
PRINTED IN THE UNITED STATES OF AMERICA 



CONTENTS 



Contributors vii 

Introduction ix 

1 The Lomas Formations of Coastal Peru: Composition and 
Biogeographic History 1 

Michael O. Dillon, Miyuki Nakazawa, and Segundo Leiva Gonzdles 

2 Response of a Land Snail Species (Bostryx conspersus) in the 
Peruvian Central Coast Lomas Ecosystem to the 1982-1983 and 
1997-1998 El Nino Events 10 

Rina Ramirez, Saida Cordova, Katia Caro, and Janine Dudrez 

3 Debris-Flow Deposits and El Nino Impacts Along the Hyperarid 
Southern Peru Coast 24 

Luc Ortlieb and Gabriel Vargas 

4 Paleoenvironment at Almejas: Early Exploitation of Estuarine 

Fauna on the North Coast of Peru 52 

Shelia Pozorski and Thomas Pozorski 

5 The Impact of the El Nino Phenomenon on Prehistoric Chimu 
Irrigation Systems of the Peruvian Coast 7 1 

Thomas Pozorski and Shelia Pozorski 

6 El Nino, Early Peruvian Civilizations, and Human Agency: 

Some Thoughts from the Lurin Valley 90 

Richard L. Burger 



Contributors 



Editors 

Jonathan Haas 

Anthropology Department 

Field Museum 

1400 So. Lake Shore Drive 

Chicago, Illinois 60605-2496 

U.S.A. 

(jhaas@fmnh.org) 

Michael O. Dillon 

Botany Department 

Field Museum 

1400 So. Lake Shore Drive 

Chicago, Illinois 60605-2496 

U.S.A. 

(dillon @ sacha.org) 

Contributors 

Richard L. Burger 

Peabody Museum of Natural History 

Yale University 

170 Whitney Avenue 

New Haven, Connecticut 06520 

U.S.A. 

(Richard.Burger@yale.edu) 

Katia Caro 

Museo de Historia Natural 

Universidad Nacional Mayor de San Marcos 

Apartado 14-0434 

Lima- 14, Peru 

Saida Cordova 

Museo de Historia Natural 

Universidad Nacional Mayor de San Marcos 

Apartado 14-0434 

Lima- 14, Peru 

Janine Duarez 

Museo de Historia Natural 

Universidad Nacional Mayor de San Marcos 

Apartado 14-0434 

Lima- 14, Peru 



Segundo Leiva Gonzales 

Museo de Historia Natural 
Universidad Privada Antenor Orrego 
Trujillo, Peru 

Miyuki Nakazawa 

Department of Biology 
Kyushu University 
6-10-1 Hakozaki, Higashi-ku 
Fukuoka 812-8581, Japan 
(chn52010@par.odn.ne.jp) 

Luc Ortlieb 

Institut de Recherche pour le Developpement 

UR Paleotropique 

32 Avenue Henri-Varagnat 

F-93143 Bondy-Cedex, France 

(Luc.Ortlieb@bondy.ird.fr) 

Shelia Pozorski 

Department of Psychology and Anthropology 

University of Texas-Pan American 

Edinburgh, Texas 78539 

U.S.A. 

(spozorski@panam.edu) 

Thomas Pozorski 

Department of Psychology and Anthropology 

University of Texas-Pan American 

Edinburgh, Texas 78539 

U.S.A. 

(tpozorski @ panam.edu) 

Rina Ramirez 

Museo de Historia Natural 

Universidad Nacional Mayor de San Marcos 

Apartado 14-0434 

Lima- 14, Peru 

(rinarm@pucrs.br) 

Gabriel Vargas 

Institut de Recherche pour le Developpement 

UR Paleotropique 

32 Avenue Henri-Varagnat 

F-93143 Bondy-Cedex, France 

(Gabriel.Vargas@bondy.ird.fr) 

Departamento de Geologia 
Universidad de Chile 
Plaza Ercilla 803 
Santiago, Chile 
(gvargas@ing.uchile.cl) 



vn 



Title-page illustration: Moche fineline painting from northern Peru 
showing a naturalistic figure in an animated reed boat. The draw- 
ing is by Donna McClelland and is reproduced from Moche Fine- 
line Painting: Its Evolution and Its Artists (UCLA Fowler Museum 
of Cultural History, 1 999) courtesy of the artist, the authors, Chris- 
topher Donnan and Donna McClelland, and the publisher. The ves- 
sel from which the drawing was made is in the collections of the 
Art Institute of Chicago. 



Introduction 



On May 28-29, 1999, a group of sixteen scientists met at the Field 
Museum in conjunction with the VIII Annual A. Watson Armour 
III Spring Symposium to discuss the impacts of the El Nino phe- 
nomenon on the biology and cultural history of coastal Peru over 
the last 10,000 years. The meeting brought together anthropolo- 
gists, archaeologists, and biologists with a shared interest in the 
effects of this potent global weather disturbance. The one-day 
workshop and subsequent symposium presented research results 
documenting the impact of this phenomenon from a wide range of 
perspectives. The papers published here represent the results of 
research from these various fields and differing points of view. 
The impact of El Nino on terrestrial and marine ecosystems has 
been well documented over the last 20 years, but the interpretation 
of these results remains controversial. The common thread linking 
most of these efforts is an attempt to date the onset of the El Nino 
phenomenon using various types of proxy data. Estimates range 
from a few thousand to tens of thousands of years. Whatever its 
age, it is obvious that El Nino had and continues to have a pro- 
found impact on the coastal environments of Peru, and more gen- 
erally of western South America. 

Michael O. Dillon 



IX 



The Lomas Formations of Coastal Peru: 
Composition and Biogeographic History 

Michael O. Dillon, Miyuki Nakazawa, and Segundo Leiva Gonzdles 



For nearly 3,500 km along the western coast of 
South America (5-30S latitude), the Atacama 
and Peruvian deserts form a continuous hyper- 
arid belt, broken only by occasional river val- 
leys from the Andean Cordillera. Native vege- 
tation of the deserts is largely restricted to a 
series of fog-dependent communities termed lo- 
mas formations, meaning small mountains. This 
chapter provides a backdrop for the subsequent 
discussions in this volume of human occupation 
in coastal Peru over the last 10,000 years. This 
requires a synthesis of the present-day coastal 
vegetation, analysis of the origins of the mod- 
ern flora, and reconstruction of past climates, 
including the onset of El Nino conditions, using 
proxy data from a variety of sources. Paleocli- 
matic data suggest that arid conditions existed 
along the coast prior to 100,000 years ago, well 
before the arrival of the first humans in western 
South America. Distributional patterns and re- 
lationships within specific members of the flora 
are discussed to help explain current conditions. 
Specifically, we have examined relationships in 
the flowering plant genus Nolana (Solanaceae), 
a group of over 80 species distributed predom- 
inantly in the lomas formations of Peru and 
Chile. The reconstructed phylogeny of Nolana 
provides a framework for examining the coastal 
lomas formations and the processes important 
in their evolution, including the effects of gla- 
cial cycles, sea level changes, and the historical 
development of the El Nino-Southern Oscilla- 
tion weather phenomenon. 



Introduction 

Much of the western coast of South America 
(5-30S latitude) is occupied by deserts, form- 
ing a continuous belt that extends for more than 
3,500 km along the western escarpment of the 
Andean Cordillera, from northern Peru to north- 
ernmost Chile. The climate and geomorphology 
of this region have been discussed in detail 
elsewhere (Dillon 1997; Ferreyra 1953; Rundel 
et al. 1991), and only a brief sketch is provided 
here for discussion purposes. The Peruvian de- 
sert is a narrow coastal band at the base of the 
Andean Cordillera that extends nearly 2,000 km 
in length but is only 50-100 km wide. The de- 
sert is interrupted only by occasional rivers that 
reach the coast, and their borders support ripar- 
ian vegetation common to the inland river val- 
leys. The factors responsible for the develop- 
ment of the hyperarid conditions include isola- 
tion from eastern weather patterns by the An- 
dean Cordillera, and temperature homogeneity 
resulting from the influence of cool sea-surface 
temperatures associated with the south-to-north 
flow of the Humboldt (Peruvian) Current. This, 
combined with a positionally stable subtropical 
anticyclone, results in a mild, uniform coastal 
climate with the regular formation of thick fogs 
below 1 000 m elevation from September to De- 
cember. 

Where the coastal topography is low and flat, 
this stratus layer dissipates inward with little bi- 
ological impact (Figs. 1 and 2A), but where iso- 
lated mountains or steep coastal slopes intercept 



M. O. Dillon et al 



o vegetation 

Tillandsia spp. 4-800 



fv" woody plants 



o:6-. o: ./ herbaceous perennials 

:<.<- 



no vegetation 
Tillandsia spp. 




Figure 1. Vegetation zonation in the fog zone or lomas formation of coastal Peru. 



the clouds, a fog zone develops with a stratus 
layer concentrated against the hillsides (Fig. 
2B). This fog, termed garua in Peru, is key to 
the floristic diversity of the unusual desert plant 
communities, termed lomas formations. In 
Peru, we estimate there are nearly 70 discrete 
localities supporting lomas vegetation (Fig. 3), 
including several offshore islands (e.g., Islas de 
Las Viejas, San Gallan, San Lorenzo). The ac- 
tual area covered by vegetation, even during pe- 
riods of maximum development, is probably 
less than 8,000 hectares. The vegetation of the 
lomas formations of Peru is unique and com- 
posed of many species that occur only in these 
small desert oases. 



Lomas Vegetation 

Lomas communities occur as islands of vege- 
tation separated by varying distances of hyper- 
arid habitat devoid of plant life. Since plant 
growth is dependent on available moisture and 
the drought tolerance of individual species, a 
combination of climate, physical topology, and 



the ecophysiology of each species of plant ul- 
timately determines community composition. 
The individual formations are highly variable 
and consist of mixtures of annuals, short-lived 
perennials, and woody vegetation. Current es- 
timates of the flora of the Peruvian lomas in- 
clude over 815 species distributed in 357 genera 
and 85 families of flowering plants. The distri- 
bution patterns of these species can be roughly 
grouped into broad categories, including (1) 
pan-tropical or weedy species, (2) long-distance 
disjunctions from the Sonora Desert or Baja 
California, (3) species disjunct from the adja- 
cent Andean Cordillera, and (4) plants restricted 
to the coastal deserts, sometimes in a single lo- 
cality. Endemism at the level of species often 
exceeds 40% in individual lomas communities. 
The greatest number of endemics are found in 
southern Peru between 15S and 18S latitude 
and include both endemic genera, such as Is- 
laya (Cactaceae), Weberbaueriella (Fabaceae), 
Mathewsia, and Dictyophragmus (both Brassi- 
caceae), and endemic species within genera, 
such as Ambrosia (Asteraceae), Argylia (Big- 
noniaceae), Astragalus (Fabaceae), Cristaria 
and Palaua (both Malvaceae), Calceolaria 



Figure 2. Atacama and Peruvian desert communities. A. Flat inland desert region devoid of plants. B. Stratus 
clouds impacting the headlands where lomas formations develop. C. Rainstorm above Cerro Campana in the northern 
Peruvian coastal desert during the 1997-1998 El Nino event, February 1998. D. Cerro Cabezon during the 1997- 
1998 event. E. Corn cultivated within the lomas formations of Cerro Cabezon in northern Peru, January 1998. F. 
Goats grazing on the abundant vegetation at Mejfa during the El Nino event, October 1983. G. A carpet of Nolana 
humifusa on the upper slopes of Cerro Cabezon, January 1998. H. Flowering individual of Nolana humifusa at Cerro 
Cabezon. 



The Lomas Formations of Coastal Peru 




M. O. Dillon et al. 



ACHENOO 
MEJIA '. 

-^ V3AMA GRANDE 



200\ 400 690 \800km 




Figure 3. Geographic features, including lomas formation localities, in the Atacama and Peruvian deserts. 



(Scrophulariaceae), Tiquilia (Boraginaceae), 
Jaltomata, Leptoglossis, and Nolana (all Sola- 
naceae), and Eremocharis (Apiaceae). 

We have examined patterns of similarity 
within the overall flora of the lomas formations 
and have found that the coastal deserts of west- 



ern South America are not uniform (Duncan 
and Dillon 1991; Rundel and Dillon 1998; Run- 
del et al. 1991). Our analysis supports three flo- 
ristic segments that appear to have independent 
histories: (1) a northern Peruvian unit from 
755'S to 12S latitude, (2) a southern Peruvian 



The Lomas Formations of Coastal Peru 



unit from 12S to 18S latitude, and (3) a north- 
ern Chilean unit from 20S to 28S. The area 
between 1 8S and 20S is nearly devoid of veg- 
etation (Rundel et al. 1991) and is suggested to 
have been a barrier to coastal dispersal for an 
extended period (Alpers and Brimhall 1988). 
Only 1 15 species, or ca. 12% of the total desert 
flora of 1,350 vascular plant species, are re- 
corded from both sides of 18S (roughly the 
Peru-Chile border). When widespread weeds 
are eliminated from that total, less than 6% of 
the native species are known from either side. 

Although the richness of the marine environ- 
ment would have provided early man with a 
primary source of sustenance (Keefer et al. 
1998), the lomas formations could also have 
acted as an important source of fresh water, 
food, and construction materials for early coast- 
al visitors and inhabitants (Lanning 1965). The 
presence of vegetation, often forageable, would 
have attracted the native camelids, for example, 
guanaco, and deer, both of which were game 
for early man. Supplies of seeds and insects 
would have made lomas sites havens for native 
bird species. The native flora does contain some 
edible fruits; for example, Jaltomata and Ly- 
copersicon, both members of the Solanaceae 
family, have tomato-like, edible berries. Edible 
roots from diverse plant families might also 
have provided some nourishment that could 
have been utilized periodically, for example, 
Argylia radiata (Bignoniaceae), Begonia octo- 
petala (Begoniaceae), Oxalis dombeii (Oxali- 
daceae), Solarium montanum (Solanaceae), and 
Tropaeolum peltophorum (Tropaeolaceae). Ag- 
riculture may also have been practiced at some 
locations, especially during exceptional years 
associated with El Nino events. Today, crops 
are cultivated in the lomas formations when op- 
portunities are provided by increased available 
moisture. Corn was planted at Cerro Cabezon 
(Fig. 2E) in northern Peru during an El Nino 
event in March 1998, and both corn and wheat 
were cultivated in the lomas between Moque- 
gua and Tacna in 1983. 

The influence of man on the lomas forma- 
tions, especially over the last 1500 years, 
should not be underestimated. Many native 
woody species have been severely depleted for 
firewood and construction. It may be assumed 
that native tree species, such as Caesalpinia 
spinosa (tara), Carica candicans (mito), or 
Myrcianthes ferreyrae, had wider distributions 
and larger populations prior to the arrival of 



man. The removal of woody vegetation almost 
certainly would have changed the extent of her- 
baceous plants. Building in many coastal areas 
has replaced lomas habitat with homes and fac- 
tories. Movement of livestock between the in- 
terior and the coast has led to the introduction 
of many Andean weeds (Sagastegui and Leiva 
1993). The historical introduction of alien or 
exotic species, such as Australian trees (Euca- 
lyptus and Casuarina), has changed the char- 
acter of the landscape. Perhaps the worst plague 
that man has set upon the lomas formations 
since the arrival of Europeans was the intro- 
duction of herbivores such as goats (Fig. 2F), 
which are very destructive to the native com- 
munities. 



El Nino Events 

In our search for the forces that act on the 
coastal regions, we identified short-term cli- 
matic fluctuations of El Nino events (5- to 50- 
year cycles) as important seasonal influences on 
the coastal region. The physics behind the El 
Nino-Southern Oscillation (ENSO) phenome- 
non is complex and represents a worldwide 
weather perturbation. El Nino conditions pre- 
vail when the normally cold waters of the coast 
of western South America are displaced by a 
warmer, western Pacific surface and subsurface 
body of water that stimulates brief periods of 
heavy rainfall (Fig. 2C) and relatively high tem- 
peratures. This influx of available moisture has 
profound effects within the lomas formations 
(Fig. 2D) and has undoubtedly helped shape 
their composition and structure. Primarily, this 
moisture stimulates massive germination of 
seeds, leading to large blooming events that re- 
plenish seed banks for annual and perennial 
plants. These events also provide opportunities 
for seed dispersal and establishment, which 
would expand distributions under favorable 
conditions (Fig. 2G). The impact of El Ninos 
on these communities is obvious (Dillon and 
Rundel 1990), and one can only wonder what 
the coastal vegetation would resemble in the ab- 
sence of these conditions. Potentially, levels of 
floristic diversity would be much lower and mi- 
gration and establishment more difficult. In the 
western Pacific, the reverse effects of recurrent 
droughts and rainfall variability have been im- 



M. O. Dillon et al. 



plicated in the evolution of vegetation patterns 
in Australia (Nicholls 1991). 

El Nino events have been recorded in both 
historical (Quinn and Neal 1987) and Holocene 
periods (DeVries 1987; Fontugne et al. 1999; 
Magilligan and Goldstein 2001; Rodbell et al. 
1999; Sandweiss et al. 1996, 1999, 2001). Lon- 
ger-term records of El Nino events are more 
difficult to detect and interpret (Moseley 1987). 
Recently, Hughen et al. (1999) detected vari- 
ability in growth patterns in fossil coral which 
they interpreted as representing El Nino-like 
conditions that may have existed for at least 
124,000 years. Our studies of modern vegeta- 
tion do not allow for estimations of the onset 
of El Nino conditions, but regardless of their 
age, they have undoubtedly played an important 
role in shaping the present coastal communities. 



Glacial Cycles and Sea Level 
Changes 

Longer-term climatic change associated with gla- 
cial cycles (13,000- to 200,000-year cycles) pre- 
dates the arrival of man and the first El Nino and 
would have been active throughout the Pleisto- 
cene (1.8 million years ago). It is estimated that 
there have been at least 20 glacial events during 
the Pleistocene, each with cycles of approximate- 
ly 200,000 years. The formation of glaciers on 
mountains and poles has caused sea levels to fluc- 
tuate dramatically (Matthews 1990). Estimates of 
sea level fluctuation range between 400 and 750 
feet (120-230 m), and this lowering would have 
significantly changed the position of the seashore 
in relation to that of today. This drop would have 
exposed a considerable area of the continental 
shelf and displaced lomas plant communities, es- 
pecially between 5S to 15S latitude (Fig. 4). 
This would have resulted in species shifting their 
ranges in relation to the near-ocean environments, 
adapting to changing conditions in situ, or under- 
going range reductions and extinction. Glacial cy- 
cles would also have had a profound influence on 
the flora and fauna of the coastal deserts by pro- 
viding geographic isolation at certain times, and 
at other times, opportunities for merging species, 
thereby allowing for gene exchange. The last gla- 
cial cycle ended ca. 13,000 years ago, and post- 
glacial vegetation patterns are comparable to 
those we find today (Dillon et al. 1995). 



Nolana Studies 

Within the lomas formations, the genus Nolana 
(Solanaceae-Nolaneae) stands out as one of the 
most wide-ranging and conspicuous elements of 
the flora (Tago-Nakazawa and Dillon 1999). 
Nolana is a genus of ca. 85 species that is large- 
ly confined to coastal Andean South America 
from central Chile to northern Peru, with one 
species endemic to the Galapagos Islands. It is 
the only genus to be encountered in nearly all 
lomas formations. Nolana species are often im- 
portant members of their respective communi- 
ties and dominate in the numbers of individuals 
present. Their showy flowers are beautiful, and 
species display various types of habits annu- 
als, perennials, or shrubs and variable corolla 
sizes and shapes (Fig. 2H). Ecologically, No- 
lana species prefer arid and semi-arid habitats, 
with their greatest concentration in near-ocean 
habitats within a few kilometers of the shoreline 
(Fig. 2G). The establishment of a phylogeny for 
Nolana has provided a framework for testing 
hypotheses of isolation events in desert com- 
munities. The species distribution pattern in No- 
lana is similar to that in the overall flora and 
displays three distinctive units: northern Peru, 
southern Peru, and northern Chile. Only four 
species have distributions that span the 18- 
20S gap. The presence of two major groups 
(clades) in the genus Nolana, one Peruvian and 
the other Chilean, points to long-term isolation 
of the genus above and below 18S latitude. 

Reliable data on speciation rates for desert 
plants are largely lacking. However, the devel- 
opment of endemic genera and species, and the 
morphological and physiological adaptations 
they manifest, support the hypothesis of long- 
term aridity along the coast of Peru, at least 
from 12S to 28S latitude (Rundel and Dillon 
1998). The timing of vicariant events (separa- 
tion) can be estimated with molecular diver- 
gence data to establish a molecular clock (Tago 
1999). For the genes investigated, all estimates 
for the first appearance of Nolana are late Ter- 
tiary (Miocene, 10.6-11.6 mya). These data 
also suggest that TV. galapagensis potentially 
reached the Galapagos Islands sometime be- 
tween 4 and 8 mya (late Miocene to early Pli- 
ocene). Because of character evolution in the 
mainland members of Nolana, it appears that 
N. galapagensis was pre-adapted to arid habi- 
tats prior to its dispersal to the island chain 
(Tago-Nakazawa and Dillon 1999). The geo- 



The Lomas Formations of Coastal Peru 




10 



12 



13 



78 



77 



76 C 



Figure 4. Bathometric diagram illustrating the continental shelf of Peru between 5S and 14S latitude. Stippled 
area indicates the land exposed should there be a 100-meter drop in sea level. Between 14S latitude (Pisco, Peru) 
and 28S latitude (northern Chile), the continental margin is very narrow. 



graphic origin of this remote island endemic re- 
mains a mystery, but comparative morphology 
points to Chilean ancestors (Dillon, unpubl.). 

Recent archeological findings from the north- 
ern Atacama Desert have recorded Nolana 
fruits (technically mericarps containing seeds) 
in rodent middens dating to 35,000 years B.P. 
(Betancourt et al. 2000). These mericarps are 
comparable to those we find in this desert lo- 
cality today. Therefore, the divergence data 
from molecular studies and the presence of No- 
lana in desert habitats for no less than 35,000 
years suggest that 10,000 years ago, the overall 



character of the coastal flora was similar to that 
found today. The frequency of strong El Ninos 
and demonstrated sea level changes suggest that 
these phenomena have played a role in stimu- 
lating evolution in the plants of the lomas for- 
mations. 



Conclusions 

The vegetation of coastal Peru is largely re- 
stricted to the lomas formations, a series of iso- 



8 



M. O. Dillon et al. 



lated, fog-dependent plant and animal commu- 
nities that are diverse and highly endemic. In- 
dividual lomas localities have unique species 
compositions and display disharmonic patterns 
found in "true" insular communities. While the 
aridity along the Peruvian coast is essentially 
constant, with negligible rainfall, the topogra- 
phy and geologic history combine to divide 
coastal Peru into a northern unit, 755'S to 12S 
latitude, and a southern unit, from 12S to 18S 
latitude. 

Given available paleoclimatic data and di- 
vergence times suggested by molecular clock 
calculations on gene sequences, it appears that 
Nolana occupied coastal desert environments in 
both Peru and Chile prior to the Pleistocene gla- 
cial events. Further investigations will be nec- 
essary to test hypotheses of the age for the de- 
sert, but our preliminary studies point to west- 
ern South America as an arid region of great 
antiquity well over 35,000 years ago. It appears 
that the flora of the lomas formations have been 
shaped by the effects of short- and long-term 
climatic changes and by the influence of man 
and introduced animals. Our data suggest sta- 
bilized aridity for coastal Peru since before the 
arrival of its first inhabitants (10,000 years 
ago), but with dynamic periods with much 
greater available moisture (Sandweiss et al. 
2001). Early man would have found an envi- 
ronment with more trees and much denser veg- 
etation, which could have provided valuable re- 
sources in the inhospitable coastal desert. 

Acknowledgments. M.O.D. acknowledges the 
support of the National Science Foundation and 
National Geographic Society for field studies 
associated with El Nino events. S.L.G. thanks 
the Field Museum Scholarship Committee for 
financial support to visit the Field Museum. F. 
Barrie, W. Burger, and P. Rundel provided con- 
structive reviews that improved the manuscript. 



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RODBELL, D. T, G. O. SELTZER, D. M. ANDERSON, M. 



The Lomas Formations of Coastal Peru 



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SAGASTEGUI-A., A., AND S. LEIVA G. 1993. Flora In- 
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SANDWEISS, D. H., K. A. MAASCH, AND D. G. ANDER- 



SON. 1999. Transitions in the Mid-Holocene. Sci- 
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Response of a Land Snail Species (Bostryx conspersus} in the 

Peruvian Central Coast Lomas Ecosystem to the 

1982-1983 and 1997-1998 El Nino Events 



Rina Ramirez, Saida Cordova, Katia Caro, and Janine Dudrez 



Land snails are conspicuous inhabitants of the 
lomas ecosystems, which are islands of vege- 
tation in the Pacific coastal desert of South 
America. The mollusks are adapted to survive 
the extreme summer conditions of the lomas, 
when the highest temperatures and the lowest 
humidities are reached. Bostryx conspersus 
(Sowerby, 1833; Mollusca, Bulimulidae) is the 
most common species from the lomas of the 
Peruvian central coast. In a year without an El 
Nino event, individuals of B. conspersus aesti- 
vate during the dry season (December-April) 
buried in the ground, mainly next to perennial 
plants. During the wet season the snails become 
active again. We present our observations of 
changes in snails' seasonal activity during the 
1982-1983 and 1997-1998 El Nino events, oc- 
curring within the lomas of Iguanil and Lachay 
(Lima, Peru), respectively. The activity of B. 
conspersus during the summer of those years 
was unusual. The snails behaved as if it were a 
wet season. They had successful recruitment 
that led to a remarkable population explosion, 
mainly due to the high humidity and increased 
shelter. However, the response of B. conspersus 
showed differences between the two El Nino 
events, reflecting dissimilarities between the 
starting time and duration of the sea-surface 
temperature anomalies and the concomitant 
weather variation in the lomas of the central 
coast of Peru. The response of B. conspersus to 
the seasonal changes during 1995 and the cold 



year of 1 996 are contrasted with those of the El 
Nino years. 



Introduction 

The coast of Peru is a desert. The terrestrial 
biodiversity, mollusks in particular, is concen- 
trated mainly in the lomas. The desert land- 
scape changes drastically during El Nino 
events, the oceanographic component of El 
Nino-Southern Oscillation (ENSO), which has 
affected the Pacific coast of South America 
since 5800 B.P. (Sandweiss et al. 1999). The 
lomas are spectacular ecosystems, islands of 
vegetation that endure the harsh conditions of 
dry summers and enjoy the humidity of the ad- 
vective fogs coming from the ocean during the 
winter. The resident fauna of the lomas is also 
adapted to its seasonality (Aguilar 1954, 1985). 
Similarly, the biota must be adapted to climatic 
changes in the mid- and long term produced by 
recurrent El Nino events or the species would 
have become extinct. However, almost nothing 
is known about the responses of terrestrial spe- 
cies to El Nino events, compared to what is 
known about the marine biota (Arntz et al. 
1985; Arntz and Fahrbach 1996; Vegas 1985). 
Among the fauna, land snails are conspicuous 
inhabitants of the lomas, and because of their 
low vagility, they are good animals in which to 
study responses to El Nino events. Following 



10 



Response of a Land Snail Species (Bostryx conspersus) 



\ 1 




Figure 1. Map showing location of the study sites, Lachay and Iguanil, Peru. 



an El Nino event (a phase with warm tropical 
water), there is a phase with cold tropical water 
called La Nina (Sandweiss et al. 1999), produc- 
ing changes in the lomas weather as well. Our 
study deals with the response of Bostryx con- 
spersus (Sowerby, 1833) to the last two major 
El Nino events (1982-1983 and 1997-1998) 
and the 1996 La Nina event in the lomas of the 
central coastal desert of Peru. 



Materials and Methods 

Study Site 

Location. The two study sites are located in 
the Department of Lima, Peru (Fig. 1 ). The lo- 
mas of Lachay (1119'S, 7722'W), a national 
reserve, are 105 km north of Lima City and 7 
km from the seashore. The altitude is between 
150 and 750 m. The lomas of Iguanil (1 123'S, 
7714'W) are located southeast of Lachay and 
103 km from Lima, 15 km from the seashore. 
The altitude is between 250 and 750 m. 



Climate. The climate of the lomas is season- 
al, characterized by a dry season (December- 
April) and a wet one, also called the "lomas 
season" (late July-September). The other 
months are transitional between seasons. Usu- 
ally the highest temperatures (monthly mean: 
20C) and the lowest humidities (79%-82%) 
are reached during summer, contrary to what 
happens during the wet season, when the mean 
monthly air temperature is 15C, with very high 
air humidity (Ordonez and Faustino 1983; Saito 
1976; Torres 1985). The El Nino events change 
this seasonal picture because of an increase in 
precipitation as drizzle or summer precipitation 
(Pinche 1994; Torres 1985). 

During an El Nino event, the sea-surface 
temperature increases abnormally above the 
mean (Fig. 2). In the continental area, air tem- 
peratures in the lomas also change, showing the 
same tendency (Fig. 3). The same tendency was 
also noticed in Lima City (Obregon et al. 1985). 
Sea-surface temperature data corresponded to 
mean monthly values from Puerto Chicama 
(0742'S, 7927'W). 



12 



R. Ramirez et al. 




Ja r M Ap My Jn J ASONDJaFMApMyJnJ A 3 O N D 



---*--- 1982-83 



1995-96 



1997-98 



Figure 2. Sea-surface temperature anomalies at the Puerto Chicama station, Peru (0742'S, 7927'W). The char- 
acterization of years follows Aguilar (1990): El Nino events: >2.7 (extraordinary), 1.7-2.7 (strong), 0.8-1.6 (mod- 
erate), 0.5-0.7 (weak). A normal year is 0.6 to 0.4. La Nina events: 0.9 (cold year), 1.8 (very cold year). 



Lomas of Iguanil During 1982-1983. The 
micrometeorologic data were recorded by CIZA 
(Arid Zones Research Center, Agrarian Univer- 
sity, La Molina, Peru). Observations were taken 
during 10 hours of 1 day a month, at altitudes 
of 300 and 500 m. We used the mean values of 
the day for air temperature, relative humidity, 
and soil humidity. Precipitation values are from 



Torres (1985) (Table 1). The climatogram is 
shown in Figure 4. 

Lomas of Lachay During 1995-1998. The 
data were acquired from SENAMHI (Servicio 
Nacional de Meteorologfa e Hidrografia del 
Peru). The data for both air temperature and 
relative humidity are mean monthly values; pre- 




SST (1982-83) SST (1995-96) 

* SST (1 997-98) - - - *- - - AT (Iguanil 1 982-83) 

- - o_ . AT (Lachay 1 995-96) - - A - - AT (Lachay 1 997-98) 



Figure 3. Comparison of sea-surface temperatures at the Puerto Chicama station and air temperatures at two 
lamas along the central coast of Peru. 



Response of a Land Snail Species (Bostryx conspersus) 



13 



TABLE 1. The lomas of Iguanil: Meteorologic and biologic data (1982-1983). 



Month, year 


Air temp. 

(C) 


Relative 
humidity (%) 


Soil humidity 
(%) 


Precipitation 
(mm)* 


Ground cover 

(%)* 


B. conspersus 
(no. snails/ 
9400 m 2 ) 


Jan. '82 (Ja2) 


23.99 


77.49 


1.18 




0.81 




Mar. '82 (M2) 






1.05 








May '82 (My2) 


22.6 


72.15 


0.85 




2.55 





July '82 (J2) 


16.05 


85.08 


0.82 




5.025 


15 


Aug. '82 (A2) 


17.89 


86.62 


5.09 




3.3 


23 


Sept. '82 (S2) 










38 




Oct. '82 (O2) 


18.42 


80.12 


3.27 




38.65 


43 


Nov. '82 (N2) 










12.5 




Dec. '82 (D2) 


24.88 


73.76 


1.895 




30 


7 


Jan. '83 (Ja3) 


26.13 


76.34 


2.49 


7 


44.15 





Feb. '83 (F3) 


24.72 


80.4 


2.815 


8 


64.3 





Mar. '83 (M3) 


27.57 


65.07 


0.915 




45.8 


6 


Apr. '83 (Ap3) 


23.59 


93.44 


6.83 


6 




94 


May '83 (My3) 


21.59 


94.14 


3.2 


5 


47.9 


24 


June '83 (Jn3) 


20.93 


96.06 




9 


75.65 




July '83 (J3) 


16.09 


93.65 


8.5 


5 


94 


118 


Sept. '83 (S3) 


16.66 


97.17 


6 




54.5 





* After Torres (1985). 



cipitation is the cumulative monthly value (Ta- 
ble 2). The climatogram is shown in Figure 5. 

Vegetation. The lomas vegetation consists of 
herbaceous species that are green mainly during 



the wet season, and also perennial species 
(shrubs and trees) that adapt to the seasonality 
of the lomas (Dillon and Rundel 1989; Ferreyra 
1993; Ono 1986). In general, changes in climate 
conditions during the year modify the landscape 



I 

X 







100 
95 
90 
85 
80 
75 
70 
65 
60 



ap3 




14 



19 24 

Temperature (C) 



29 



Figure 4. Climatogram of the lomas of Iguanil, Peru, 1982-1983. 



14 



R. Ramirez et al. 



TABLE 2. The lomas of Lachay: Meteorologic and biologic data (1995-1998). 



Month, year 


Air temp. Relative humidity Precipitation 
(C) (%) (mm) 


RGC* B. conspersus 
(%) (no. snails/400 m 2 ) 


Jan. '95 (Ja5) 


21.2 


89 


3.5 






Feb. '95 (F5) 


22.1 


85 


0.5 






Mar. '95 (M5) 


21.2 


84 


1.4 






Apr. '95 (Ap5) 


19.9 


86 








May '95 (My5) 


18.4 


86 


0.7 






June '95 (Jn5) 


16 


92 


2 






July '95 (J5) 


13.5 


97 


19.9 


72 





Aug. '95 (A5) 


13.2 


98 


4.7 


1271 


3 


Sept. '95 (S5) 


14 


97 


17.2 


1492 


69 


Oct. '95 (O5) 


14.5 


96 


10.5 


456 


85 


Nov. '95 (N5) 


15.8 


92 


1.6 


681 


54 


Dec. '95 (D5) 


16.5 


89 


1.4 





207 


Jan. '96 (Ja6) 


18.4 


88 


1.1 





21 


Feb. '96 (F6) 


22.5 


82 







20 


Mar. '96 (M6) 


22.1 


79 







7 


Apr. '96 (Ap6) 


19.3 


81 


0.4 





7 


May '96 (My6) 


16.4 


88 







31 


June '96 (Jn6) 


13.2 


98 





278 


43 


July '96 (J6) 


14.2 


97 









Aug. '96 (A6) 








368 


89 


Sept. '96 (S6) 








147 


60 


Oct. '96 (O6) 








39 


12 


Nov. '96 (N6) 


15.7 


91 





2 


25 


Dec. '96 (D6) 


18.2 


89 








10 


Jan. '97 (Ja7) 


21 


95 









Feb. '97 (F7) 


22.2 


93 









Mar. '97 (M7) 


22.6 


97 











May '97 (My7) 













July '97 (J7) 


19.1 


96 


10.7 





3 


Aug. '97 (A7) 


18.1 


95 


31.7 


211 


8 


Sept. '97 (S7) 


18.1 


93 


40.4 


1345 


6 


Oct. '97 (O7) 


17.4 


92 


28.4 


927 


13 


Nov. '97 (N7) 


18.9 


93 


20.4 


373 


2 


Dec. '97 (D7) 


21.2 


94 


65.2 


237 


5 


Jan. '98 (Ja8) 


23 


96 


103.1 


476 


220 


Feb. '98 (F8) 


23.6 


95 


47.5 


980 


552 


Mar. '98 (M8) 


23.7 


91 


6 


724 


637 


Apr. '98 (Ap8) 


22.3 


88 


2.5 


321 


146 


May '98 (My8) 


18.9 


93 


16.5 


325 


897 


June '98 (Jn8) 


16.4 


98 


34.5 


529 


1587 


July '98 (J8) 


15.4 


97 


16.4 


907 


1473 


Aug. '98 (A8) 


14 


99 


46.4 


763 


5448 


Sept. '98 (S8) 


14.1 


99 


28.2 


806 


9369 



* Reiterated ground cover. 



from a brown color (almost zero ground cover) 
during summer to a vivid green color during 
winter, when the annual species provide a large 
amount of ground cover. However, during El 
Nino events, the timing of these changes is very 
different, as was observed during the 1982- 
1983 El Nino event in Iguanil (Torres 1985) and 
in 1997-1998 in Lachay (Arana et al. 1998). 
Ground cover data for Iguanil are from Torres 
(1985). We used the mean values for each 
month (Table 1). For Lachay, we used the "re- 



iterated ground cover" figure obtained by the 
botanical team from the Museum of Natural 
History of the University of San Marcos (Table 
2). 

Mollusks. Bostryx conspersus (Sowerby, 
1833; Gastropoda, Bulimulidae) has a globose 
and rather thin shell of about 15 mm height 
(Fig. 6c). It has been recorded in the lomas of 
central and southern Peru (Departments of 
Lima and Arequipa) (Aguilar and Arrarte 1974; 



Response of a Land Snail Species (Bostryx conspersus) 



15 



E 

3 
I 



100 
95 
90 
85 



SL 80 



75 




12 



16 



20 



24 



Air Temperature (C) 



Figure 5. Climatogram of the lomas of Lachay, Peru, 1995-1998. 




Figure 6. Some lands snails from Lachay: a, Succinea peruviana; b, Bostryx modestus; c, Bostryx conspersus; 
d, Scutalus proteus; e, Scutalus versicolor; f, Bostryx scalariformis. (Photograph by B. Collantes.) 



16 



R. Ramirez et al. 



Weyrauch 1967). Individuals of B. conspersus 
aestivate during the dry season buried in the 
ground, mainly next to perennial plants. They 
are also found buried adjacent to rocks, or in 
small interstices between them. During the wet 
season the snails become active again (Pulido 
and Ramirez 1982; Ramirez 1988). 

B. conspersus shares the lomas with other 
land snail species. For example, in Lachay the 
following native species are also present: Bos- 
tryx aguilari Weyrauch, 1967; B. modestus 
(Broderip, 1832) (Fig. 6b); B. scalariformis 
(Broderip, 1832) (Fig. 6f); Scutalus proteus 
(Broderip, 1832) (Fig. 6d); Scutalus versicolor 
(Broderip, 1832) (Fig. 6e); Succinea peruviana 
Philippi, 1867 (Fig. 6a); and the two minutes 
Pupoides paredesi (d'Orbigny, 1835) and Gas- 
trocopta pazi (Hidalgo, 1869), as well as the 
introduced Helix aspersa (Miiller, 1774). 



Monitoring 

Lomas of Iguanil. The study area in the lo- 
mas of Iguanil was the Quebrada El Granado. 
The quantitative survey was carried out 1 day 
a month in a transect of 20 X 470 m (= 9,400 
m 2 ) between 420 and 600 m above sea level. 
The transect is located in a hilly area along the 
center of the ravine, with perennial vegetation 
(mainly shrubs, e.g., Trixis cacalioides, 
Ophryosporus pubescens, Cestrum auriculatus, 
Dicliptera tomentosa, Heliotropium spp.). 
There is also annual herbaceous vegetation 
(e.g., Nicotiana paniculata, Chenopodium pe- 
tiolare, Oxalis sp., Sicyos baderoa). The survey 
was carried out from May 1982 to July 1983 
(except June 1983). The search for unburied 
snails was conducted by direct observation. R. 
Ramirez carried out this part of the work as a 
member of a team of the CIZA/UNA-La Mo- 
lina (Lima, Peru), which conducted botanical, 
faunal, and anthropological research in several 
lomas of the central coast of Peru during the 
1970s and 1980s. 

Lomas of Lachay. The Museum of Natural 
History of the University of San Marcos, Lima, 
Peru, has been engaged in monitoring vegeta- 
tion and mollusks to track El Nino events in the 
lomas ecosystems as part of the RIB EN study 
(Red de Impacto Biologico de los Eventos El 
Nino, CONCYTEC) from May 1995 to the 
present. 



For a quantitative survey, we selected an area 
dominated by shrubs (e.g., Ophryosporus pe- 
ruvianus, Senecio spp., Trixis cacalioides, Cro- 
ton spp.), including annual herbaceous vegeta- 
tion (e.g., Loasa urens, Nicotiana paniculata, 
Urocarpidium peruvianum, Nolana humifusa). 
Monitoring of the land snails at the two lomas 
was carried out as independent projects. Al- 
though we tried to maintain the same area in 
Lachay for quantitative sampling as in Iguanil, 
it did not work as well because of the greater 
abundance of B. conspersus. We delimited four 
plots of 10 X 10 m (= 400 m 2 ), 50 m apart, 
along a transect between 470 and 550 m in al- 
titude. We counted the unburied snails observed 
in 1 day per month, except during 1998, when 
we needed an extra day because of the high 
number of individuals and the exuberant her- 
baceous vegetation. The data we present here 
are from July 1995 to September 1998. No sur- 
vey was conducted in July 1996 or in January, 
February, April, or June of 1997. 



Principal Component Analysis 

We used principal component analysis (PCA) to 
ascertain whether changes in monthly density 
of B. conspersus along with changes in air tem- 
perature, relative humidity, or ground cover 
could help discriminate El Nino months from 
non-El Nino months. We did not use the pre- 
cipitation data, which were incomplete. Micro- 
soft Excel was used for data management and 
the analyses were performed using SPSS (Sta- 
tistical Package for the Social Sciences, V05) 
software. 



Results 

Iguanil (1982-1983) 

The monthly variation in number of unburied 
individuals of Bostryx conspersus in the lomas 
of Iguanil did not show the same trend from 
one year to the next. In 1982 the snails were 
active during part of the winter and spring, 
whereas in 1983 the activity period started ear- 
lier, at the end of the summer. The highest num- 
ber of snails recorded in 1983 was recorded ear- 
lier, in July, and was almost threefold (118 in- 
dividuals in 9,400 m 2 ) the number recorded in 



Response of a Land Snail Species (Bostryx conspersus) 



17 



1982 (October, 43 individuals) (Table 1, Fig. 
7a). 

In relation to the differences among survey 
months, PCA of data on snails, ground cover, 
air temperature, and relative humidity generated 
four components to explain the total variance. 
The PCI analysis explained 62.157% of the 
variance, with variation in number of snails 
having the greatest influence, followed by var- 
iation in the relative humidity. In the PC2 anal- 
ysis (28.492%) ground cover was the principal 
factor, followed rather distantly by air temper- 
ature (Table 3). In the scatter diagram of PCI 
X PC2, three groups of months are formed, 
with the months of the 1982-1983 El Nino ep- 
isode in two of them (December 1982-March 
1983, and May-July 1983) (Fig. 8). 



Lachay (1995-1998) 



During the almost 4 years of survey of B. con- 
spersus in the lomas of Lachay, the higher num- 
ber of active snails (unburied) per observation 
period decreased from 1995 through 1997, but 
in 1998 exceeded the highest counts of previous 
years. The lowest numbers of snails occurred 
during the summer of 1996 and the summer of 
1997, corresponding to the aestivation period 
(Table 2, Fig. 7b). 

In relation to the differences among the sur- 
vey months, PCA generated four components 
to explain the total variance, of which the first 
two accounted for 71.412% of the variance. In 
PCI (52.046%), variation in relative humidity 
had the greatest influence, followed by variation 
in air temperature, while in PC2 (19.366%), the 
number of snails and the ground cover were the 
variables with greatest influence (Table 4). In 
the scatter diagram of the first two components, 
five groups of months were formed. Those of 
the 1997-1998 El Nino segregated into two 
groups (March-July-August 1997, and Septem- 
ber-December 1997-January-April 1998); the 
following months (post-El Nino) also formed a 
separate group (June-September 1998). The 
two other groups were formed by (1) August- 
November 1995 and (2) December 1995-Jan- 
uary-May 1996 and November-December 
1996 (Fig. 9). 



Discussion 

Bostryx conspersus has seasonal behavior, 
showing a clear response to the seasonal cli- 
mate of the lomas ecosystem (Pulido and Ra- 
mirez 1982; Ramirez 1988). The intensity of 
change in the climatic regimen can be detected 
from the variation in monthly number of un- 
buried snails, as described here. El Nino events 
change the seasonality of the lomas, mainly be- 
cause of summer rains (Oka and Ogawa 1984; 
Pinche 1994). 

Climatologically, no one year was similar to 
any other during the study (Figs. 4 and 5), nor 
were the monthly density variations in active 
land snails similar (Fig. 7). Analysis of the sea- 
surface temperature anomalies at Puerto Chi- 
cama during the periods of our studies (1982- 
1983, 1995-1998) (Fig. 2; Quispe 1993) shows 
that in this respect too, there were not two equal 
years (Rasmusson and Arkin 1985). This dem- 
onstrates the direct influence of the ocean on 
the climate of the lomas as well as other con- 
tinental areas (Obregon et al. 1985). Likewise, 
we cannot say that during the period of survey 
in the lomas of Lachay there was a "normal" 
year for the lomas. On the contrary, we had the 
El Nino years (1997-1998), an unusually cold 
year (La Nina, 1996), and a mixed warm and 
mildly cold year (1995). 

Using the data of B. conspersus along with 
those of air temperature, relative humidity, and 
ground cover, then performing a principal com- 
ponent analysis, we arrived at assemblages of El 
Nino months that were arranged in a different 
way from those of non-El Nino ones. At the 
same time, months during El Nino events were 
segregated into two groups; we call them the first 
phase and the second phase of El Nino (Figs. 8 
and 9). Checking the anomalies of sea-surface 
temperature, it is also possible to see that the two 
El Nino events were indeed different. 

The 1982-1983 and 1997-1998 El Nino ep- 
isodes are considered to be extraordinary be- 
cause the sea-surface temperature anomalies 
differed by more than 2.7 SD (Fig. 2) (Aguilar 
1990; Quinn 1993). At the same time, the El 
Nino events differed in starting point and in du- 
ration. For example, in the 1982-1983 El Nino 
event, warm water reached the central coast of 
Peru late in 1982 November in Callao (Go- 
mez 1985) and did not affect the wet season 
of the year very much. B. conspersus showed a 
typical seasonal behavior during that year. The 



18 



R. Ramirez et al. 



140 
120 -I 
100 

80 

60 

40 

20 




10000 



1000 
o 

I 

1 100 

i 



b)[ 



O Lachay 95-96 



Lachay 97-98 



Figure 7. Monthly density of unburied individuals of Bostryx conspersus in two lomas on the central coast of 
Peru: a, Iguanil; b, Lachay. 



second instance of warming of the sea-surface 
water occurred during the fall of 1983 April- 
July (Zuta et al. 1985) which brought more 
precipitation to the lomas, marking an early be- 
ginning of the wet season in 1983 (Fig. 10). The 
usual brown landscape of the summer was re- 
placed by a nice carpet of herbaceous vegeta- 
tion (Torres 1985). The population of B. con- 
spersus from the lomas of Iguanil also respond- 



ed to the quasi-lomas season, the difference be- 
ing that the air temperatures were higher than 
during the winter wet season (Fig. 4). The bi- 
ological impact on the snails was positive; the 
snails awoke earlier from the aestivation period, 
and the recruitment was successful (Ramirez 
1984). The population reached the levels of the 
previous wet season very early (Fig. 7). A pos- 
sible reason for this could be the survival of 



TABLE 3. Results of PCA for the lomas of Iguanil (1982-1983). 



Initial Eigenvalues 



Compo- 




% of 


Cumula- 


Component 


nent 


Total 


Variance 


tive % 


Variables 


1 


2 


3 


4 


1 


2.486 


62.157 


62.157 


Air temperature 


-0.801 


0.561 


0.165 


0.127 


2 


1.140 


28.492 


90.649 


Relative humidity 


0.872 


-0.197 


0.444 


0.052 


3 


0.332 


8.302 


98.951 


Ground cover 


0.495 


0.860 


0.074 


-0.099 


4 


0.042 


1.049 


100.000 


Bostryx conspersus 


0.916 


0.214 


-0.319 


0.115 



Response of a Land Snail Species (Bostryx conspersus) 



19 




-2 



-1 

PCI (62.157%) 



Figure 8. Plots of the first two principal components for the months May 1982 to July 1983 for the lomas of 
Iguanil. 



more eggs and snails (especially just hatched 
and juveniles) than usual (Ramirez 1984) be- 
cause of the high humidity (the main cause of 
death is desiccation [Pollard 1975]) and more 
available shelter (Lomincki in Pollard 1975) be- 
cause of the high amount of annual vegetation. 
The two instances of sea-surface warming 
during the 1997-1998 El Nino event occurred 
earlier than those of the 1982-1983 El Nino 
event. The first arrival of the warm water was 
early during the fall of 1997 (Fig. 2). The whole 
year was abnormally warm in the lomas, and 
during the winter the high relative humidity val- 
ues characteristic of the "lomas season" were 
never reached; the contrary happened during 
the late spring, which had high relative humid- 
ity values, as shown in the climatogram for La- 



chay (Fig. 5). The characteristic herbaceous 
vegetation of the wet season was negatively af- 
fected. For example, Isemene amancaes had 
both a late beginning and a short development 
period during 1997 (Agiiero and Suni 1999). 
The population of B. conspersus was also neg- 
atively impacted. Most of the snails stayed bur- 
ied, and those that "woke up" were more ex- 
posed to desiccation. As a consequence, the re- 
cruitment was very poor (Fig. 1 1 ). The second 
occurrence of warming of the 1997-1998 El 
Nino event was at the beginning of the summer 
of 1998 (Fig. 2) and brought an unusual amount 
of water to the lomas (Fig. 12), extending the 
late wet season of 1997 into the summer of 
1998. Here the impact of the El Nino event was 
positive for B. conspersus, which showed a 



TABLE 4. Results of PCA for the lomas of Lachay (1995-1998). 



Initial Eigenvalues 




Compo- 




% of 


Cumula- 


Component 


nent 


Total 


Variance 


tive % 


Variables 


1 


2 


3 


4 


1 


2.082 


52.046 


52.046 


Air temperature 


-0.707 


0.218 


0.622 


0.255 


2 


0.775 


19.366 


71.412 


Relative humidity 


0.833 


0.160 


-0.076 


0.524 


3 


0.704 


17.602 


89.014 


Ground cover 


0.698 


0.578 


0.288 


-0.308 


4 


0.439 


10.986 


100.000 


Bostryx conspersus 


0.633 


-0.606 


0.478 


-0.064 



20 



R. Ramirez et al. 




-2 



-1 



1 

PCI (52.046%) 



Figure 9. Plots of the first two principal components for the months July 1995 to September 1998 for the lomas 
of Lachay. 



population explosion. The recruitment was very 
successful; and that, along with the high hu- 
midity and exuberant herbaceous vegetation 
(Arana et al. 1998, 1999), led to a high survival 
rate among the snails. 

The cold year of 1996 (La Nina) had a rel- 
atively negative impact on B. conspersus com- 
pared with the maximum number of snails 
counted in the 1995 "wet season." The weather 
was colder and drier than during the other years 



(Figs. 5 and 12). The mortality rate of individ- 
uals of all size classes was high, and the re- 
cruitment was poor (Fig. 1 1 ; Ramirez et al. 
1999). Affected in this way, the population ex- 
perienced an El Nino the following year (1997), 
with a hot winter and without the characteristic 
high humidities (Fig. 5), depleting the popula- 
tion even more. Finally, the arrival of the sec- 
ond phase of the 1997-1998 El Nino event in- 
jected some life into B. conspersus. The range 



10 -, 
9 

! ?: 
























10 
9 
8 ^ 
7 






















9 







c 6 
o 

j= 5 

a 4 














1 








1 


r 





5 E 
4 I 


,, 

o 3^ 
Q- 2 












/ 


f 






^>' 


, ^ 
\ 






3 o 
2 W 


1 - 
















I 










V 






1 



*^ v\ J ^"1 ^r* fiiL-J *^ w\ J ^5 
XT V*^ ^ oP ^J 
\ 

^^ 


\=n PRECIPITATION (mm) 


-o SOIL HUMIDrTY (%) 



Figure 10. Precipitation and soil humidity in the lomas of Iguanil, 1982-1983 (measured 1 day per month). 



Response of a Land Snail Species (Bostryx conspersus) 



21 



10000 



1000 



100 




>15mm 



10.1 -15mm -A-5-10mm 



-<5mm 



Figure 11. Structure of the population of Bostryx conspersus by size classes from August 1995 to September 
1998 in the lomas of Lachay. The El Nino event occurred from May 1997 to April 1998. (After Ramirez et al. 1999.) 



of the population expanded as far as the her- 
baceous vegetation did. The post-El Nino 
months following the 1997-1998 event coincid- 
ed with the 1998 wet season, which resulted in 
an even higher density of active B. conspersus. 
This was probably also the case for 1995 (end 



of a weaker but much longer-lasting El Nino 
than the two episodes analyzed here). Precipi- 
tation and ground cover were greater than in 
1996 (Table 2, Fig. 12), and B. conspersus 
reached higher densities than in 1996 and 1997 
(Figs. 7b and 9). 



100 
















c 
"5. 



. 40 




| 




















20 


* 


. . .1, 


1 


J 


i 






nJ 


i 




D 




* * > 


b << 


> * ^ ^ > * * 


Lachay (1995-96) 


D Lachay (1997-98) 



Figure 12. Precipitation in the lomas of Lachay, 1995-1998 (cumulative monthly values). 



22 



R. Ramirez et al. 



Thus, although the two El Nino episodes dif- 
fered from each other, they were similar in that 
their second phase had a positive impact on the 
biota. The increase in humidity led to an in- 
crease in herbaceous vegetation, and both of 
these factors contributed to an increase in the 
population of B. conspersus. At the same time, 
predation on this population, mainly by rodents 
and birds, also increased (Ramirez et al. 1999). 

Acknowledgments. The work carried out on 
the lomas of Iguanil was possible thanks to the 
Arid Zones Research Center of the Agrarian 
University (CIZA-UNA, La Molina, Peru). Di- 
ana Silva y Juan Torres facilitated the work at 
Iguanil. The monitoring of land mollusks on the 
lomas of Lachay was made possible with the 
aid of the American States Organization 
(through RIBEN-CONCYTEC), the University 
of San Marcos (FEDU-UNMSM), and the Na- 
tional Council of Science and Technology 
(CONCYTEC). We are grateful to the Institute 
Nacional de Recursos Naturales for permits to 
perform research in the National Reserve of La- 
chay. Jose Arenas, Sergio Cano, Doris Florin- 
dez, Marisa Ocrospoma, and Maria Samame 
participated enthusiastically in the fieldwork, 
and Asuncion Cano and Cesar Arana provided 
the data on ground cover. Finally, we thank Ser- 
gio Solari and Sonia Valle, who helped prepare 
the illustrations. 



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Nino. CONCYTEC, Lima, Peru. 



Debris-Flow Deposits and El Nino Impacts 
Along the Hyperarid Southern Peru Coast 

Luc Ortlieb and Gabriel Vargas 



The coastal regions of Ecuador, Peru, and Chile, 
which today experience the strongest meteoro- 
logic and oceanographic impacts of El Nino, 
are also the areas where paleoclimatologic re- 
search is likely to yield relevant information 
about former El Nino processes. The extreme 
aridity that characterizes the coast of southern 
Peru and northern Chile is favorable for the rec- 
ord of episodic rainfall events that induce floods 
and debris flows and the subsequent preserva- 
tion of these deposits. This chapter compiles 
available instrumental, documentary, and geo- 
logic data on such deposits formed along the 
coast at 17-18S latitude and discusses the re- 
lationships that can be inferred between dated 
debris-flow deposits and the occurrence of El 
Nino events. The approach thus involves an 
analysis of temporal correlations between El 
Nino events, debris-flow episodes, and instru- 
mental measurements of rainfall data during the 
last several decades. This analysis shows a 
weak statistical correlation between monthly or 
yearly rainfall amount and the warm phase of 
El Nino-Southern Oscillation (ENSO), but also 
that strong rainfall, sufficient to provoke debris 
flows, generally occurs during El Nino years. 
Documentary data from the last few centuries 
also tend to indicate that heavy rainfall episodes 
along the coast of southern Peru have common- 
ly occurred during El Nino years, even though 
many El Nino years did not experience rains. 
We conclude that, for at least the last few cen- 
turies, El Nino conditions have been favorable 
for the formation of exceptionally short-lived 
but intense rainfalls, but that these conditions 
are not sufficient per se. Several regional and 
local meteorologic mechanisms and situations 



are apparently involved in the episodic occur- 
rence of strong rainfalls and debris-flow activity 
along the coast of southern Peru. 

Debris-flow activity during the early Holo- 
cene and at the end of the Pleistocene, when 
regional hydrologic conditions were different 
than at present, is more difficult to interpret in 
relation to ENSO. Unlike previous authors, we 
consider that debris-flow deposits formed prior 
to the mid-Holocene do not constitute strong 
enough evidence for past El Nino conditions. 
Similarly, we presume that lack of debris-flow 
evidence during a given time period cannot be 
taken as an indication that no El Nino events 
occurred during that period. Until we have a 
better understanding of the meteorologic pro- 
cesses driving exceptional intense rainfalls in 
the area and of the paleohydrologic regime, it 
would be misleading to infer the existence of 
El Nino, or La Nina, conditions from the exis- 
tence of debris-flow deposits in this particular 
region. 

The Relevance of Paleo-ENSO 
Studies 

El Nino Southern Oscillation, or ENSO, is the 
main source of global ocean climate variability 
on an interannual time scale. Understanding the 
variability of ENSO through geologic time is 
necessary to determine the boundary conditions 
that drive the phenomenon, to examine the in- 
terrelationships between this mode of ocean cli- 
mate variability and other, longer-term sources 
of climate change, and to constrain coupled 
oceanic-atmospheric models. There is also 



24 



Debris-Flow Deposits and El Nino Impacts 



25 



strong societal interest in improved forecasting 
of El Nino events and in estimating the intensity 
and frequency of future ENSO events under 
conditions of global warming. Moreover, stud- 
ies of the evolution of the dynamics of the 
ENSO trough time are necessary to better un- 
derstand the influence of the ocean climate sys- 
tem on the development of different cultures 
around the world. 

Because instrumental records have been 
maintained for only a short time, whereas cli- 
mate modelers require longer-term records, 
there is a growing need for paleo-ENSO proxy 
records such as coral reef sequences, ice cores, 
dendroclimatic analyses, lacustrine and alluvial 
sedimentary sequences, beach ridge series, and, 
for the last few centuries, documentary data. 
These different proxy records generally aim to 
reconstruct the frequency and intensity of for- 
mer El Nino events the warm phase of ENSO. 
Up to now, however, none of these records by 
itself has yielded a complete series of El Nino 
occurrences. For instance, Quinn and collabo- 
rators (Quinn et al. 1987; Quinn and Neal 1992; 
Quinn 1993) provided historical El Nino se- 
quences based on documentary data that have 
been widely used by ENSO researchers. But 
other researchers (Hocquenghem and Ortlieb 
1992; Whetton and Rutherfurd 1994; Whetton 
et al. 1996; Ortlieb 1998, 1999, 2000; Ortlieb 
et al. 2002) have questioned the accuracy of 
many so-called reconstructed El Nino events 
between the sixteenth and the eighteenth cen- 
turies. This is not surprising, because some of 
the documentary data come from areas as far 
away as the Nile delta, China, and South Amer- 
ica, where ENSO teleconnections are moderat- 
ed by other atmospheric and oceanic processes. 
As a result, no consensus has been reached on 
a historical El Nino (or ENSO) chronological 
sequence prior to the instrumental record. At 
longer time scales the problem is still more 
acute, if for different reasons: the scarcity of 
high-resolution sequences, geochronological 
uncertainties, alteration or partial erosion of the 
records, and so on. In all cases, for very recent 
(documentary) or older (geologic) records, one 
particular problem must be addressed: Which 
regions record the former occurrences of the 
phenomenon with highest reliability? How can 
we be sure that a geographic area that today 
satisfactorily registers ENSO anomalies also 
did so in the past, under different regional and 
global circulation patterns? 



El Nino Manifestations in Peru and Chile 

The El Nino phenomenon was first identified in 
northern Peru, near the border with Ecuador 
(Carranza 1891), as the combination of an 
anomalous seasonal (summer) warming of the 
coastal waters and heavy rainfall in the desert 
of Sechura (4-6S). Later, it was observed 
along the coast of southern Ecuador to central 
Chile that the phenomenon is also characterized 
by a lowering of the thermocline and the nu- 
tricline and by a rise in sea level that may reach 
several decimeters within several weeks. The 
coast of northern Peru is where the El Nino 
phenomenon provokes the highest sea level rise 
(more than half a meter in 1982-1983), greatest 
seawater warming (up to 10C at Paita, in 
1982-1983), and greatest rainfall anomalies (lo- 
cally up to 4,000 mm, compared to 100 mm 
mean). It is thus natural that this region is fa- 
vored in the search for paleo-El Nino evidence 
(Quinn et al. 1987; DeVries 1987; Ortlieb and 
Machare 1993; Machare and Ortlieb 1993). 

Another favorable area that faithfully regis- 
ters the occurrence and intensity of ENSO man- 
ifestations is central Chile (Quinn and Neal 
1983). Rutllant and Fuenzalida (1991) showed 
that at least since the end of the nineteenth cen- 
tury, the warm phase of ENSO is characterized 
by an excess of winter precipitation and the 
cold phase is generally marked by a deficit of 
rainfall. Over the last 120 years, for which there 
are reliable instrumental rainfall data, there is a 
good correlation between El Nino in northern 
Peru (during the austral summer) and central 
Chile (during the preceding austral winter) (Ort- 
lieb 1998, 1999, 2000; Ortlieb et al. 2002). This 
coincidence reflects a teleconnection mecha- 
nism involving large-scale atmospheric pro- 
cesses in the eastern Pacific region (Caviedes 
1981; Hastenrath 1985; Hamilton and Garcia 
1986; Deser and Wallace 1987; Aceituno 1988, 
1990; Philander 1991; Allan et al. 1996). It is 
because of this teleconnection that Quinn et al. 
(1987) and Quinn and Neal (1992) relied on 
documentary data on historical climatic anom- 
alies from either central Chile or northern Peru 
to reconstruct past occurrences of El Nino 
events. However, Ortlieb and co-authors (Ort- 
lieb 2000; Ortlieb et al. 2002) noted that before 
1817, very few heavy rainfall events recon- 
structed from documentary evidence from 
northern Peru and central Chile did coincide in 
time. Ortlieb (1997, 1998, 2000) thus suggested 



26 



L. Ortlieb and G. Vargas 



that the teleconnection mechanisms had possi- 
bly been affected by other modes of climatic 
variability, such as those related to the Little Ice 
Age. This hypothesis remains to be further test- 
ed, for example, by comparing with data from 
tropical ice core and coral reef sequences. 
Meanwhile, it is plausible that the regional te- 
leconnections observed today may not have 
been operating in past centuries and millennia. 



When Did the El Nino Phenomenon Appear 
in Peru? 

In the last few decades, there has been some 
discussion regarding the onset of the El Nino 
system of climate variability in Peru. Sandweiss 
and co-authors (Sandweiss 1986; Rollins et al. 
1986; Sandweiss et al. 1983, 1996, 1999) pro- 
posed that no ENSO manifestation was recorded 
in Peru before the mid-Holocene and supported 
the hypothesis that the onset of the El Nino oc- 
curred at about 5000 B.P. This interpretation re- 
lied heavily on observations that some warm- 
water mollusks occurred in different localities 
prior to 5000 B.P. (noncalibrated age) along the 
coast of north-central Peru. The mentioned au- 
thors suggested that a large reorganization of the 
ocean-atmosphere circulation system in the east- 
ern Pacific took place during the mid-Holocene. 
They claimed that prior to 5000 B.P., the coastal 
waters of that area were significantly warmer 
than today, and that after the mid-Holocene, the 
boundary between the cold Humboldt (Peru) 
Current and the warm equatorial waters would 
have moved northward by about 500 km, to 
reach its present position (at about 5S). 

Other researchers (DeVries and Wells 1990; 
Diaz and Ortlieb 1993; Perrier et al. 1994; Bearez 
et al. 2003) have not shared the interpretation that 
coastal waters were warmer in the past in north- 
central Peru and instead have argued that the 
warm-water molluscan species were all lagoonal 
forms that lived in protected, marginal lagoons 
that provided a higher temperature than the open 
ocean. Other biological proxy data also failed to 
support the theory of a major shift of the bound- 
ary between the cool Humboldt domain and the 
warm equatorial waters. Perrier et al. (1994) 
showed through stable isotope serial analyses that 
Trachycardium shells from north-central Peru dat- 
ed to 5500 B.P., 5800 B.P., and 6100 B.P. contained 
growth irregularities similar to those observed to- 
day in response to El Nino events, registering 



short-term thermal anomalies of the water that 
amounted to several degrees C (like those record- 
ed after the very strong 1982-1983 El Nino 
event). Furthermore, DeVries et al. (1997) argued 
that it was precisely because the El Nino system 
already existed before 5000 B.P. that the lagoons 
which formed during mid-Holocene maximum 
sea level, near 7000 B.P. (Wells 1988), could be 
fed episodically with larvae of warm-water spe- 
cies that normally live in the Panamic molluscan 
Province (i.e., north of 6S). Similar conditions of 
lagoonal environments that previously enabled the 
survival of extralimital warm-water species have 
also been found in deposits of prior interglacial 
stages in southern Peru and northern Chile (Ort- 
lieb et al. 1990, 1996; Diaz and Ortlieb 1993; 
Guzman et al. 2001). 

Recently, additional terrestrial proxy data have 
tended to indicate that El Nino extended back to 
the end of the Pleistocene, although with differ- 
ent characteristics. Rodbell et al. (1999) reported 
data from a high-elevation Andean lake in south- 
ern Ecuador, whereas Keefer et al. (1998) pre- 
sented data from alluvial and debris-flow depos- 
its in southern Peru (Fig. 1). Both studies suggest 
that ENSO mechanisms were not restricted to the 
second half of the Holocene. However, both 
studies relied on an interpretation of alluvial pro- 
cesses in two quite different depositional envi- 
ronments, and both assumed that present-day hy- 
drologic phenomena linked to ENSO were also 
operative at the end of the Pleistocene and in the 
early Holocene. 

Here we evaluate interpretations of climatic 
significance of alluvial deposits formed in the 
southernmost part of the Peruvian coastal des- 
ert. To what extent can we assume, as Keefer 
et al. (1998) did, that remnants of debris flows 
and floods in the coastal region of southern 
Peru were related to El Nino conditions in the 
latest Pleistocene and early Holocene times? 
The relationships between paleo-ENSO impacts 
and alluvial and debris-flow deposits in the area 
will be analyzed at different time scales with 
different kinds of data: ( 1 ) for the last half-cen- 
tury, using instrumental measurements; (2) for 
the last few centuries, based on documentary 
sources; and (3) for the last 12,000 years, using 
radiocarbon-dated geologic deposits. Recently 
acquired data from southern Peru are presented 
and discussed with respect to other published 
El Nino proxy data (Keefer et al 1998; Fontug- 
ne et al. 1999). 



Debris-Flow Deposits and El Nino Impacts 



27 



Piu 



Lima 
< 13mm 






Iquique 


t 




Rainfall (mm) 






V ^ 


JH : n tu 


Antofagasta 





V 


H 1020-2030 






\1 


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1 510-760 




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[250-510 
1 0-250 


< 13 mm / 




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_] iJ 



Pacific Ocean 

Ilo 




Quebrada Tacahuay 
j- 1 8S Punta El Ahogado 
72W Quebrada Los Burros 

Quebrada El Cation 
100km 



Hi"' 
Rio San Jose 



B 



Figure 1. A. Location of sites studied in southern Peru and northern Chile, with indication of mean interannual 
rainfall (modified from Kendrew 1961). B. Details of the coast of southernmost Peru, with localities studied. 



El Nino Impact on Rainfall and 
Debris-Flow Events in Southern 
Peru During the Second Half of the 
Twentieth Century 

El Nino and Rainfall Anomalies in Peru 

After the very strong 1982-1983 El Nino event, 
which was characterized by a severe drought in 
the southern half of Peru and on the Bolivian 
Altiplano, many authors (e.g., Huaman Solis 
and Garcia Pena 1985; Francou and Pizarro 
1985; Garcia Pena and Fernandez 1985; Rope- 



lewski and Halpert 1987; Thompson et al. 
1984) considered that the precipitation deficits 
in this area were typical of El Nino conditions. 
At present it is considered that the relative 
drought that was observed during El Nino years 
may be more specific to the Andean part of 
southern Peru, and not precisely specific to the 
coastal region of southern Peru (Rome-Gaspal- 
dy and Ronchail 1998). Recent analyses of in- 
strumental rainfall data from the second half of 
the twentieth century confirm that the positive 
rainfall anomalies over the coastal regions of 
Ecuador and northern Peru exhibit the only sta- 



28 



L. Ortlieb and G. Vargas 



tistically significant correlation with El Nino 
events within the region encompassing Ecuador, 
Peru, and Bolivia (Aceituno 1988; Rossel 1997; 
Rome-Gaspaldy and Ronchail 1998; Rossel et 
al. 1998). Analysis of monthly rainfall data be- 
tween 1960 and 1990 indicates that only the 
coastal area of northern Peru (Piura region) 
shows a positive correlation between rainfall 
and the warm phase of ENSO, and intensified 
drought during the cold phase of ENSO (La 
Nina) (Rome-Gaspaldy and Ronchail 1998). 
More specifically, no clear correlation between 
rainfall anomalies and ENSO (either the El 
Nino or the La Nina phase) has been observed 
for the southern Peru region (Minaya 1994; 
Rome-Gaspaldy and Ronchail 1998). The very 
strong 1982-1983 El Nino event was charac- 
terized by intensified drought in Arequipa and 
a strong deficit of the Majes River flow (17,058 
km 2 watershed, 450 km long, spring at 4886 m 
on the western flank of the Andean Cordillera), 
but other strong El Nino events, such as the 
1972-1973 event, were marked by exceptional 
rainfall at Arequipa and maximum flows of the 
Majes River (Minaya 1993, 1994) (Fig. 2). 
These inconsistencies are linked to complex cli- 
matic mechanisms operating in this particular 
region involving a variable position of the In- 
tertropical Convergence Zone, substantial dif- 
ferences in the atmospheric circulation patterns 
during different ENSO events, and interactions 
between the coastal area and the cordilleran 
zone. 



Debris-Flow Episodes and Strong Rainfalls 
in Southern Peru 

In arid countries, debris-flow activity is tightly 
linked to the occurrence of relatively intense 
rainfalls. In the Chile-Peru coastal desert, de- 
bris-flow activity may be observed with precip- 
itation amounts above 20 or 30 mm, and after 
rainfall episodes that last more than 3 hours 
(Vargas et al. 2000). 

The occurrence of heavy rainfall episodes, 
debris flows, and inundations of the coastal re- 
gion of Tacna (southern Peru) was compared 
with available monthly rainfall data, informa- 
tion obtained from local newspapers, and 
ENSO indexes for the period 1960-2000. The 
mean annual rainfall at Tacna for this period 
was 19 mm. The total annual rainfall data and 
the annual mean Southern Oscillation Index 



(SOI) do not show any significant correlation. 
However, a coincidence between years with an 
excess of rainfall and low values of SOI (Fig. 
3) was observed. On the other hand, not all the 
years characterized by low SOI values exhibit 
an annual excess of rainfall. Between 1960 and 
2000, there were 1 1 "rainy" months (rainfall > 
19 mm per month). Three of them (September 
1960, September 1961, and September 1962, 
with 20.2, 34.6, and 33.0 mm of total accu- 
mulation, respectively) do not correlate with El 
Nino events (as defined by Trenberth 1997). For 
the rest of the cases (January 1983 and January 
1998, with respectively 24.0 mm and 21.2 mm 
total rainfall; July 1963 and July 1972, with re- 
spectively 32.0 mm and 59.0 mm total rainfall; 
September 1963, September 1965, and Septem- 
ber 1997, with respectively 33.1, 22.6, and 31.7 
mm total rainfall; and December 1997, with 
28.2 mm of total rainfall), a correlation is ob- 
served with El Nino events as defined by Tren- 
berth (1997). During La Nina episodes, -an ex- 
cess of precipitation events has not occurred. 

Information published in local newspapers in 
Tacna allows a historical reconstruction of the 
heavy rainfall episodes and debris flows in this 
region for the last 40 years (Table 1). In the 1 1 
months with heavy rainfall previously men- 
tioned, debris flows occurred in January 1983 
and September 1997, and to a lesser extent in 
July 1972 and January 1998. In these cases, the 
heavy rainfall episodes occurred during El Nino 
events of strong intensity, characterized by low 
SOI values and important anomalies of the sea- 
surface temperature at Puerto Chicama (Table 
1, Fig. 4). The chronicles indicate a great spatial 
variability in the total amount of precipitation 
related to the strong convective character of the 
storms. During these heavy rainfall events, as 
was shown for the coast of northern Chile by 
Vargas et al. (2000), the rain frequently oc- 
curred at night. 

A similar relationship between heavy rainfall, 
debris flows, and El Nino events was deter- 
mined for the coastal area of the Atacama des- 
ert, and particularly at Antofagasta (23S), in 
northern Chile (Vargas et al. 2000). In northern 
Chile, not all El Nino events provoke "heavy" 
rainfall episodes, but all the events able to pro- 
duce debris flows (rain intensity > 20 mm/3 
hours; Hauser 1997; Vargas et al. 2000) oc- 
curred during the development phase of El Nino 
events, in the austral winter (Rutllant and Fuen- 
zalida 1991; Garreaud and Rutllant 1996). In 



Debris-Flow Deposits and El Nino Impacts 



29 




Figure 2. Comparison of annual streamflow anomalies of Majes River (southern Peru) and variation in the 
Southern Oscillation Index (SOI) during the 1950-1991 period (streamflow data from Corporation de la Aviaci6n 
Civil, CORPAC, in Minaya 1994). No clear-cut correlation is observed between El Nino (negative SOI values) or 
La Nina (positive SOI values) and the Majes River streamflow. 



1925, 1930, 1940, 1982, 1987, and 1991, heavy 
rainfall episodes in northern Chile were linked 
to storms coming from mid-latitude regions. 

In the coastal area of southern Peru, the cli- 
matic mechanisms involved in the generation of 
"heavy" rainfall events are not yet totally un- 
derstood. While debris-flow events related to 
heavy rainfall episodes were contemporary with 
strong El Nino events (Fig. 4), some of them 
occurred during the austral summer (January 
1983 and January 1998), while others occurred 
during the austral winter or spring (July 1972 
and September 1997). The strong rainfall events 
occurring in the coastal area during the austral 
summer should be linked to the activity of the 
rainy season on the Altiplano and the cordillera. 
Those occurring in winter during El Nino years 
are not clearly understood and cannot be readily 
related to the same processes described in 
northern Chile (frontal systems coming from 
mid-latitude regions). 

Because the reliable instrumental data cover 
a relatively short time period, we investigated 
the relationship between regional strong rain- 
falls and ENSO during the last few centuries. 



Historical Rainfall Data and 

El Nino Manifestations During the 

Last Four Centuries 

Documentary data on climate in Peru and Chile 
were largely used by Quinn et al. (1987), Quinn 
and Neal (1992), Hocquenghem and Ortlieb 
(1992), and Ortlieb (1999, 2000) to try to es- 



tablish a sequence of El Nino events during the 
last few centuries. Documentary sources consist 
of reports on droughts, river flooding, the de- 
struction of bridges and buildings, good and 
poor crops, heavy storms, and other impacts of 
meteorologic conditions. Information was ob- 
tained from a variety of official, ecclesiastical, 
and particular documents left by the Conquis- 
tadores and the later inhabitants of these regions 
during colonial times and after independence 
from Spain. These data led to different inter- 
pretations by the above-mentioned authors. 
Whereas Quinn tended to interpret reports of 
storms and heavier rainfall than usual along the 
coastal desert of Peru or in central Chile as ev- 
idence of past El Nino conditions, Ortlieb 
(2000) considered that only information on pre- 
cipitation excess in coastal northern Peru and in 
central Chile could be reliably used as an El 
Nino indicator. Hocquenghem and Ortlieb 
(1992) and Ortlieb (2000) argued that, based on 
instrumental records of the last decades, Rimac 
River floods (in Lima) and unusual vegetation 
cover along the coast of southern Peru should 
not be taken by themselves as evidence of El 
Nino conditions. Unusual vegetation growth in 
the lomas (hilltops) in the area of Ilo could be 
due to intensified winter garuas (coastal fogs), 
not necessarily to strong rainfall. In some cases 
it was shown that droughts in coastal northern 
Peru were coeval with vegetated lomas in 
southern Peru, probably during La Nina con- 
ditions. 

Previous work on documentary sources on 
climate anomalies in the Norte Grande of Chile 
showed that reliable data for the scarcely in- 



30 



L. Ortlieb and G. Vargas 



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Debris-Flow Deposits and El Nino Impacts 



31 





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Debris-Flow Deposits and El Nino Impacts 



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habited Atacama desert were for practical pur- 
poses limited to the last two centuries (Ortlieb 
1995). However, some additional and fragmen- 
tary data from northernmost Chile and southern 
Peru have recently turned up (Ortlieb 2000). Ta- 
ble 2 presents data gathered on unusual rainfall 
and debris-flow activity in the coastal areas of 
southern Peru and (present-day) northernmost 
Chile (north of 23S) since the earliest docu- 
mentary record, dated 1619. Information on 
heavy rainfalls in the central depression of 
northern Chile, and floods in the quebradas 
coming from the cordillera, which are linked to 
La Nina conditions in the Altiplano and the An- 
dean Cordillera, were not considered (unless 
they co-occurred with precipitation anomalies 
along the coast). The precipitation excesses are 
compared with past occurrences of El Nino (or 
La Nina) events as proposed by Quinn and Neal 
(1992), Ortlieb (2000), and Ortlieb et al. (2002). 
The last three columns of Table 2 do not con- 
tain all the reconstructed El Nino (and La Nina) 
events (according to the cited authors) but only 
those that are contemporaneous with the hydro- 
logic anomalies indicated in the first two col- 
umns at left. 

Table 2 shows that most heavy rainfall epi- 
sodes and debris-flow activity registered in the 
coastal study area occurred during El Nino 
years, as determined by either one or all of the 
cited authors. Several cases of flooding of the 
San Jose or Azapa Rivers at Arica are not re- 
lated to rainfall in the coastal area but reflect 
precipitation excess in the Andean Cordillera, 
during La Nina (or normal) conditions. 

The historical data presented here cannot be 
regarded as definitive, for several reasons. First, 
documentary data are inherently fragmentary 
and subject to error, exaggeration, and misin- 
terpretation. Second, we still lack a reliable 
chronological sequence of El Nino occurrences, 
as evidenced by conflicting accounts in the last 
three columns of Table 2. Third, the informa- 
tion on river floods does not always show the 
effects of cordilleran versus coastal rains. Rain- 
fall in the upper part of the watersheds, in both 
southern Peru and northern Chile, follows dif- 
ferent regimes and has quite different mecha- 
nisms from precipitation in the coastal areas. 
Nevertheless, the historical data presented in 
Table 2 tend to confirm that in a longer term 
than the last few decades, precipitation excess 
in the studied coastal area was generally ob- 
served during El Nino years, and that El Nino 



34 



L. Ortlieb and G. Vargas 




-1.5 



to to to <o <o 



Total annual rainfall at Tacna: 1960-2000 



>^^v 

!I 
II 

<u -a 

S 2 












Jan Mar May Jul Sep Nov 
Mean monthly rainfall at Tacna: 1960-2000 

Figure 3. A. Comparison of total annual rainfall at Tacna and SOI during the 1960-2000 period (monthly rainfall 
data from SENAMHI, Peru). B. Distribution of the mean monthly rainfall at Tacna for the same period. 



conditions do not systematically induce rainfall 
excess in the study area. 

During the last centuries, as during the last 
decades, intense rainfalls and debris-flow activ- 
ity often occurred during El Nino years, but the 
relationship is not as tight as for the coast of 
northern Peru. The "intense" rainfalls on the 
coast of southern Peru are linked to convective 
features, which may be favored by one or an- 
other side effect of the anomalous patterns of 
atmospheric circulation induced by ENSO in 
the region. 



near Punta El Ahogado, a sequence of debris- 
flow deposits yielded a new radiocarbon data 
set. 

A comparison of the geomorphic contexts 
and chronological data at these three localities 
may provide insight into the geologic and pa- 
leohydrologic processes during the Pleistocene- 
Holocene boundary and in the first half of the 
Holocene. The following discussion considers 
to what extent the debris-flow units may be re- 
lated to former occurrences of the El Nino phe- 
nomenon. 



The Latest Pleistocene/Early 
Holocene Debris-Flow Episodes 

Several localities on the coast of southern Peru 
recently yielded new data on the age of late 
Quaternary debris flows. Most of the radiocar- 
bon data was obtained from material of an- 
thropic origin: charcoal fragments, organic mat- 
ter, and marine shells. One study (Keefer et al. 
1998) has addressed the sequence of latest 
Pleistocene early Holocene alluvial deposits on 
the bank of the deeply incised Quebrada Taca- 
huay, 40 km south of Ilo (see Fig. IB). In an- 
other study, Fontugne et al. (1999) examined 
the alluvial sequence at Quebrada Los Burros, 
30 km to the south of Tacahuay. In between, 



The Quebrada Tacahuay Sequence 

Keefer et al. (1998) Data. In a locality south 
of Ilo, on the northern bank of Quebrada Ta- 
cahuay (1750'S, 7107'W), Keefer et al. (1998) 
studied a geologic section atop an inland allu- 
vial fan that encompasses the late Pleistocene- 
mid-Holocene period. The section exposes 19 
debris-flow and flood deposits, with the most 
recent of them bearing remains of human oc- 
cupation (including charcoal fragments, bird 
bones, and a few marine shells) (Fig. 5). Keefer 
et al. (1998) distinguished four periods in this 
sequence: 

Before an archaeological horizon at 12,700 



Debris-Flow Deposits and El Nino Impacts 



35 




n 5 

O -3 < 



Figure 4. Total monthly rainfall at Tacna and sea- 
surface temperature anomalies at Puerto Chicama for 
periods with occurrence of debris-flow events or in- 
undations along the coast of southern Peru. 




5290 BP 

8655 BP 

9435 BP 

>^ /10.560BP 

\ 4 \10.895BP 



( 12,490 BP 
< 1 2.670 BP 
* 12,730 BP 



Debris flow 

Sheetflood or channel flood 

Aeolian 

Midden 

Occupation layer (aeolian 

with water-laid silt) 

Desiccation crack filled with 
aeolian sand 



Figure 5. Composite stratigraphic sequence of 
the Quebrada Tacahuay. south of Ilo (from Keefer et 
al. 1998). Ages are expressed in calibrated years (cal. 
B.P.). Units Kl, K2, K3, K4cl, K4c2. K6, and K7 are 
described as debris flows. Unit K8 is the main occu- 
pation layer. Radiocarbon data from this sequence are 
shown in Table 3. 



cal. B.P., a sequence of eight debris-flow de- 
posits, three aeolian sand layers, and two ma- 
jor flood units. From an infrared-stimulated 
thermoluminescent (TL) dating at 38.2 ka at 
the base of this sequence, Keefer et al. (2001) 
later inferred that these 10 debris-flow and 
alluvial events occurred between 38,200 ka 
and 12,700 cal. B.P. 

Between 12,500 cal. B.P. and about 8800 cal. 
B.P., four extensive debris-flow deposits were 
formed (their units 2, 3, 6, and 7 [see Fig. 6], 
which we will refer to here as K2, K3, K6, 
and K7). 

Between 8800 and 5300 cal. B.P., they rec- 
ognized one debris-flow unit, which can be 
subdivided into two thin layers (subunits 
K4cl and K4c2, observed in a single profile) 
overlying an aeolian sand unit (K4c3). 
At ca. 5300 cal. B.P. (= 4550 60 B.P.) one 
last major debris-flow deposit (unit Kl) 
formed just before the main channel of Que- 
brada Tacahuay began to be incised. 

Presently, the floor of Quebrada Tacahuay 



lies about 30 m below the top of the sedimen- 
tary sequence. This sequence, cut by the paved 
coastal road, is located about 1 km inland from 
the shoreline. 

In their study, Keefer et al. (1998) empha- 
sized the archaeological aspects of their find- 
ings. The major and oldest human occupation 
was dated to 12,700-12,500 cal. B.P. and was 
apparently interrupted because of the occur- 
rence of a large debris flow (unit K7; see Fig. 
5). The archaeological remains, including a 
well-preserved hearth, which are found in a 10- 
to 50-cm-thick layer of water-laid silt, with in- 
terstratified lenses of aeolian fine sand (unit K8 
in Fig. 5), are atypical because they include 
very few marine shells, abundant seabird bones, 
some remnants of pelagic fishes, and a few lith- 
ic artifacts. 

Our Data. During a brief visit to this locality 
(in 1998), observation and sampling were con- 
ducted in the southwestern part of the area stud- 
ied by Keefer et al., to the west of the road. 
Figures 6 and 7 show the studied sequence, 



36 



L. Ortlieb and G. Vargas 




Debris-Flow Deposits and El Nino Impacts 



37 



ll 




38 



L. Ortlieb and G. Vargas 



with units numbered Tl to T6 from bottom to 
top. The upper layer, designated T6 (equivalent 
to unit Kl of Keefer et al. 1998) is a thick de- 
bris-flow deposit that is colored dark by abun- 
dant organic matter. Below it occur (from top 
to bottom) a composite debris-flow deposit 
(T5), an alluvial (sheet flood) unit (T4), another 
debris-flow unit (T3), a composite alluvial layer 
(T2), and a coarse fluvial conglomerate (Tl). 
Radiocarbon data (Table 3) were obtained on 
the two alluvial layers T2 and T4, both water- 
laid deposits that incorporate a high amount of 
reworked aeolian sand. Unit T4 contains char- 
coal fragments, seemingly related to washed- 
out hearths; marine shells brought by man; and 
abundant terrestrial gastropods (not necessarily 
linked to a human occupation). This unit T4 
includes remnants of a relatively young phase 
of human occupation dated to about 9000 cal. 
B.P. and referred to as "the shell midden" by 
Keefer et al. (1998). Unit T2, which is practi- 
cally devoid of marine shells and contains many 
bird bones, is the major "occupational" layer 
of Keefer et al. (1998) that is, their unit K8. 
Our chronological data and those of Keefer 
et al. are presented in Table 3. 

Paleohydrologic and Paleoclimatologic In- 
terpretations. The Quebrada Tacahuay se- 
quence thus consists in a succession of alluvial 
and sheet flood units, debris-flow deposits, and 
aeolian sand units. The water-laid sediments 
can be separated in two categories: the alluvial 
units, which were deposited in the bed (or the 
banks) of the Tacahuay river, and the debris- 
flow and sheet flood units, which are linked to 
superficial runoff, not necessarily within the 
valley. The dark brown (T6) or reddish (T5 and 
T3) colors of the debris-flow units (Fig. 6) re- 
sult from the proportions of clay, silt, and re- 
worked soil in the matrix; the larger size com- 
ponents may be subrounded to angular. The al- 
luvial units are generally gray or yellowish; 
their matrix is coarse-grained, and they include 
pebbles and blocks of varying size, which may 
be rounded to subangular. The sheet flood de- 
posits generally consist of thin layers or lenses 
of sands that show current figures, laminations, 
cross-bedding structures, and the like. They 
may include layers bearing reworked material 
(shells, bones, charcoal fragments). 

The petrographic composition and the shape 
of the coarse elements found in the thickest al- 
luvial units of the sequence clearly indicate that 



the material comes from upstream in the rela- 
tively large watershed of the Quebrada Taca- 
huay. Because the watershed is of limited size, 
there is no doubt that the hydrologic regime 
was controlled by rainfalls in the coastal region. 
The >25-m-thick sequence of (mainly) alluvial 
deposits that predate the T1/K9 unit (Fig. 7) 
corresponds to a late Pleistocene episode of ac- 
tive, aggrading, sedimentation processes. It is 
inferred that the hydrologic regime was con- 
trolled by regular and abundant rainfalls. The 
scarcity of chronological data from the Pleis- 
tocene sequence (besides the 38.2 ky TL date 
obtained by Keefer et al. 2001) hampers any 
precise paleoclimatic and paleohydrologic in- 
terpretation. 

The debris-flow units are mainly formed 
from superficial material eroded from the to- 
pographic surface, including interfluves and 
nearby hill slopes. The formation of these de- 
posits implies that relatively strong and intense 
rainfalls occurred in the immediate vicinity of 
the outcrops. The debris-flow units have a lim- 
ited lateral extension. As shown in Figure 7, the 
debris-flow unit T6/K1 formerly extended on 
both northern and southern sides of the present- 
day thalweg of Quebrada Tacahuay. This ob- 
servation provides a maximum age (5290 cal. 
B.P.) for the beginning of the incision of the 
quebrada at this locality. We surmise that the 
downcutting of the thalweg responded more di- 
rectly to retrogradation processes of the incision 
related to the mid-Holocene high sea level than 
to paleoclimatologic factors. Sometime around 
5000 cal. B.P. linear erosion took over the up- 
ward aggradation processes, at this locality rel- 
atively close to the coastline. We interpret that 
it was not precisely because of a variation in 
the hydrologic regime that the thalweg was 
formed and progressively entrenched. This is 
not easy to demonstrate because the erosive 
processes dominated during the second half of 
the Holocene, and thus no subsequent sedimen- 
tary deposit was preserved in this locality. In 
other words, the morphologic evolution of the 
locality during the late Holocene prevents us 
from making any comparisons between present 
(or recent) hydrologic conditions and those that 
existed prior to the mid-Holocene. 

Keefer et al. (1998) interpreted as evidence 
for El Nino manifestations the half-dozen epi- 
sodes of debris-flow events (units K7 to Kl, 
Fig. 5) identified between 12,500 and 5300 cal. 
B.P. They further suggested that, because of the 



Debris-Flow Deposits and El Nino Impacts 



39 



Quebrada El Canon 




Holocene eolian sand 



Late Pleistocene aljuvial sequence 

~S" JtSK 1 , 





Figure 8. Late Pleistocene coarse alluvial units overlain by an early Holocene sandy layer and by a late Holocene 
occupational horizon (sand and silts with abundant charcoal and ceramic fragments) in Quebrada El Canon, about 1 
km south of Quebrada Los Burros, southern Peru. The Pleistocene alluvial units are most probably coeval with those 
of Quebrada Tacahuay and with the oldest debris-flow deposits of Punta El Ahogado. 



sedimentologic similarity between these debris- 
flow deposits and those that predate unit K8 
(i.e., older than 12,700 cal. B.P.) in the sequence 
of Quebrada Tacahuay, El Nino conditions were 
also present during the late Pleistocene. These 
interpretations are essentially based on the as- 
sumption that, as at present, violent rainfalls in 
this coastal area would characteristically have 
occurred during El Nino years. 

We disagree with the interpretations of Kee- 
fer et al. regarding the character of ENSO prox- 
ies of the debris-flow units. Too little is known 
about the morphoclimatic and paleohydrologic 
local conditions at the end of the Pleistocene in 
the Tacahuay region, and more generally in 
coastal southern Peru. The superposition of 
sheet flood, debris-flow, and alluvial sediments 
has no modern equivalent and does not repre- 
sent climatic conditions comparable to present 
conditions. Instead, the abundance of alluvial 
layers for the late Pleistocene part of the Ta- 
cahuay sequence suggests a more humid cli- 
mate, with stronger and more regular flow ep- 
isodes, than in the late Holocene. If this was the 



case, there is no reason to infer that debris-flow 
activity was linked to El Nino conditions. 



Quebrada Los Burros Area 

Fontugne et al. (1999) also addressed the prob- 
lem of the local impact of El Nino during the 
Holocene. Their study was performed in the 
framework of another archaeological project 
centered on Quebrada Los Burros, an early Ho- 
locene site located some 40 km south of Taca- 
huay (see Fig. IB) (Lavallee et al. 1999). Ac- 
cording to Fontugne et al. (1999), two major 
debris-flow deposits (huaycos) were formed in 
Quebrada Los Burros: the oldest one occurred 
around 8980 cal. B.P. (between QLB2: 8160 
70 B.P. and QLB3: 8040 105 B.P., conven- 
tional ages), and the youngest one was dated to 
slightly after 3380 cal. B.P. (see Table 3). Be- 
tween these two units, ten layers of organic 
matter and pseudo-peat accumulations were in- 
terstratified (Fig. 8). These layers were inter- 
preted by Fontugne et al. (1999) as representing 



40 



L. Ortlieb and G. Vargas 



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42 



L. Ortlieb and G. Vargas 



more humid spells, with a typical duration of 
less than 200 years. Such episodes of "in- 
creased soil moisture" would have been linked 
to reinforcements of winter fogs and enhance- 
ments of the coastal upwelling strength. Fon- 
tugne et al. thus infer that no El Nino would 
have occurred between 8970 and 3380 cal. B.P. 

It must be noted that after 3380 cal. B.P., no 
other debris-flow deposit was recorded in Los 
Burros valley. 

In this case, as at Tacahuay, the previous au- 
thors suggest that debris-flow activity is typical 
of El Nino conditions, to the point that lack of 
a debris-flow deposit would imply that no El 
Nino event occurred. Again, we disagree with 
this interpretation. 

Quebrada Los Burros is a small drainage sys- 
tem surrounded by bare bedrock, particularly in 
the lower part of the valley. There is scarce su- 
perficial soil material susceptible to be re- 
worked by runoff during violent rainfalls. 
Therefore, we consider that the lack of debris- 
flow deposit during a given time period should 
not be interpreted as an indication of absence 
of intense rainfall. This view is supported by 
the fact that a strong local rainfall in mid-Sep- 
tember 1997 (see Table 1), during an El Nino 
year, did not generate a characteristic deposit in 
Quebrada Los Burros, although it produced a 
debris-flow event less than 2 km to the south, 
in the small Quebrada El Canon. 

The formation of two debris-flow deposits in 
Quebrada Los Burros reflected the occurrence 
of strong rainfalls in the valley, but it still re- 
mains to establish that the rainfalls were related 
to El Nino conditions. The organic-rich layers 
interstratified between the two debris-flow units 
indicate that humid conditions persisted for 
some time in the valley, but these conditions 
might have been related to a natural (or possi- 
bly man-made) dam downstream, in the valley. 
Such a feature, which can be inferred from the 
remnants of tuffa and carbonate concretions 
stuck to the bedrock, may have maintained an 
artificially high base level within a portion of 
the valley. Hence, the existence of pseudo-peat 
deposits in the center of the thalweg may not 
be directly linked to paleoclimatologic factors. 

The sedimentary histories of Quebrada Ta- 
cahuay and Quebrada Los Burros show little 
correspondence. The oldest debris-flow unit of 
the latter seems to have been almost contem- 
poraneous with the K2 unit of the former (see 
Table 2). 



In Quebrada El Canon, immediately to the 
south of Quebrada Los Burros (see Fig. IB), a 
complex sedimentary sequence is found that 
begins with a thick series of coarse alluvial de- 
posits and resembles the Pleistocene part of the 
Tacahuay sequence (Fig. 8). In Quebrada El 
Canon at least a dozen superposed alluvial units 
of comparable thickness (about 20 cm each) 
suggest a vigorous alluvial activity of this river, 
comparable to that of Quebrada Tacahuay. No 
radiocarbon date has yet been obtained for this 
series, but the alluvial sequence can be assigned 
to the Pleistocene because it underlies a major 
unit of aeolian sand containing human bones 
dated to 9830 140 B.P. (uncalibrated) (Fon- 
tugne and Lavallee, pers. comm., 1999). It is 
interesting to note that a similar phase of aeo- 
lian sand deposition (involving enhanced wind 
activity) also occurred near the Pleistocene-Ho- 
locene transition in the Antofagasta area, 700 
km to the south (Llagostera 1979; Vargas 1996; 
Vargas and Ortlieb 1998). 

The informal name of "El Canon" was given 
to this quebrada because of a deep incision cut 
into the >50-m-thick sand dune that was built 
up along the coastline at that time, and which 
obstructed the mouth of the river. The "canon" 
is thus the result of the erosive action of the 
strongest floods that occurred in the Holocene. 
The last time that a flood flowed through the 
canon was during the 1997-1998 El Nino event. 



El Ahogado Sequence 

The El Ahogado sequence of debris-flow de- 
posits, which is located halfway between Que- 
brada Tacahuay and Quebrada Los Burros, was 
revisited recently (after a preliminary study in 
1990). This sequence, observed in a roadcut 
(Fig. 9), lies on an interfluve between two small 
quebradas at the foot of the 600-m-high coastal 
range. It consists of a succession of at least 15 
debris-flow units. These units, which are 10 to 
30 cm thick, can be described as mud flows that 
incorporate unsorted material from upslope 
floating in a silty matrix. The reworked clasts 
are angular to subrounded, ranging in size from 
a few millimeters to 50 cm in diameter. The 
sedimentologic characteristics of the deposits 
clearly indicate that they resulted from mass 
flow of limited energy that reworked superficial 
clasts from the alluvial fans accumulated at the 
foot of the nearby range. They were formed 



Debris-Flow Deposits and El Nino Impacts 



43 




during strong rainfall episodes that struck the 
coastal region proper, which, in the area, ex- 
tends only some 3 or 4 km between the range 
itself and the coastline. 

A particularity of this locality is that a few 
debris-flow units overlie remnants of anthropic 
activity that can provide radiocarbon dates, and 
thus the maximum ages of the respective geo- 
logic deposits. The third youngest debris-flow 
unit overlies a layer with abundant marine 
shells, bird remains, terrestrial mollusks, rope 
fragments, and charcoal. Three charcoal frag- 
ments from this horizon yielded calibrated ages 
of ca. 3764, 3780, and 3946 cal. B.P. (Table 3). 
We can therefore infer that the deposit was 
formed sometime after 3760 cal. B.P. Similarly, 
the fourth youngest unit overlies a relatively 
thin, sandy layer that includes a few anthropic 
remains and many bird remains; charcoal frag- 
ments from this horizon yielded a date of 7573 
cal. B.P. (Table 3). The maximum age of this 
penultimate debris-flow deposit can thus be es- 
timated to be around 7570 cal. B.P. 

This last finding suggests that at least one 
other debris-flow episode occurred between the 
two events dated at Quebrada Los Burros (3380 
and 8970 cal. B.P.; Table 3). The 14 C date ob- 
tained on the youngest anthropic layer does not 
preclude that the youngest debris flow of Punta 
El Ahogado (<3760 cal. B.P.) was contempo- 
raneous with the youngest one identified at 
Quebrada Los Burros (ca. 3380 cal. B.P.). No 
geochronological data are available from the 
older debris flows in the El Ahogado sequence. 

One other observation, made in a comparable 
sequence located 600 km to the north of this 
locality, provides useful information. In a road- 
cut located at km 737 of the Panamerican High- 
way, 40 km north of Ocona, at Playa Muerta 
(see Fig. 1A), anthropic remains with charcoal 
fragments dated to 9130 and 9006 cal. B.P. (Ta- 
ble 3) were found below the fourth youngest 
debris-flow units (Fig. 10). Because of the sim- 
ilarity of the geomorphic situation of the El 
Ahogado and Playa Muerta debris-flow se- 
quences, we surmise that the two last-formed 
units in each locality were coeval. The oldest 
debris-flow units observed at El Ahogado are 
probably of Pleistocene age. 

Because of its morphologic location, on an 
interfluve, the El Ahogado sequence cannot 
provide a record of latest Holocene debris-flow 
activity. The small quebrada located immedi- 
ately to the south of the locality attracted most 



L. Ortlieb and G. Vargas 




'.'; V 1 "- 



m 737 Panamerican Hwy. 



Figure 10. Alluvial sequence of debris-flow deposits at Playa Muerta, southern Peru. 



of the debris-flow sediments in the course of 
the last few millennia. 



Regional Correlation of Debris- Flow 
Remnants 

The geochronological data from the four local- 
ities Quebrada Los Burros, Quebrada Taca- 
huay, Punta El Ahogado, and Playa Muerta 
in the southern Peru coastal region suggest that 
some of the alluvial and debris-flow units may 
be contemporaneous. Table 4 recapitulates the 
available data and shows a tentative lateral cor- 
relation between the four sequences. 

The latest Holocene debris-flow episode ob- 
served in Quebrada Los Burros and the third 
youngest unit at El Ahogado are younger than 
3380 cal. B.P. The previous dated event, youn- 
ger than 5290 cal. B.P., was identified in Que- 
brada Tacahuay, and may have been preserved 
at El Ahogado as well. An older event, appar- 
ently of strong intensity, might be represented 
in three localities (Playa Muerta, Tacahuay, and 
El Ahogado) and can be dated to ca. 8660 cal. 



B.P. The previous ones were all dated in the 
Quebrada Tacahuay locality and would have oc- 
curred around 9440, before 10,560, before 
10,920, at some time between 10,920 and 
12,490, and before 12,490 cal. B.P. The locali- 
ties of Tacahuay, El Ahogado, and El Canon 
recorded a series of at least 15 alluvial events 
before 12,500 cal. B.P. 



Discussion 

Debris-Flow Significance in Northern Chile 
and Southern Peru 

The extreme aridity of the coastal area of south- 
ern Peru favored the formation and subsequent 
preservation of debris-flow deposits. The narrow 
coastal plain at the foot of several high rocky 
mountain ranges, the general lack of soil cover, 
the abundance of hill-slope material available for 
transport, and the episodic character of extreme- 
ly rare rainfall events all contributed to debris- 
flow activity in this region. Sequences of piled- 
up debris-flow deposits in areas at the foot of 



Debris-Flow Deposits and El Nino Impacts 



45 



steep alluvial fans or near small quebradas are 
a particularity of the coastal region of southern 
Peru and northern Chile. Thick sequences of 
such deposits were studied in the Antofagasta 
area (23S), in northern Chile (Vargas 1996; Var- 
gas and Ortlieb 1998). It was shown there that 
the hydrologic and meteorologic conditions al- 
lowing debris-flow activity were set up during 
the middle Holocene (around 5600 cal. B.P.) and 
that no debris-flow deposition seems to have oc- 
curred in the early Holocene (Vargas et al. 2000; 
Vargas 2002). Available information on late 
Pleistocene sedimentary deposits in the Antofa- 
gasta region suggests that moderate and possibly 
regular rains, unable to provoke debris-flow de- 
posits (like those produced under present-day 
conditions), fell during the Late Glacial Maxi- 
mum (Vargas 1996; Vargas and Ortlieb 1998). 
The Pleistocene-Holocene transition was 
marked in the bay of Antofagasta by the accu- 
mulation of an aeolian sand sheet that shows 
strong wind activity. 

Along the southernmost coast of Peru, the 
geologic record of the late Quaternary suggests 
a different story than the paleohydrologic re- 
construction proposed for the Antofagasta re- 
gion. We saw that in southern Peru, debris-flow 
units were formed in the late Pleistocene, the 
Pleistocene Holocene transition, and the early 
Holocene. The record of debris-flow activity 
during the second half of the Holocene is lim- 
ited, in contrast to the existence of relatively 
thick sequences of debris-flow units found in 
some localities of the Antofagasta area. These 
differences are interesting and lead us to pro- 
pose new interpretations regarding the mecha- 
nisms involved in the formation of debris-flow 
deposits and their causal relationship with 
ENSO conditions in both regions. 

In the coastal area of northern Chile, the oc- 
currences of strong rainfall events, able to pro- 
duce debris-flow activity, are clearly linked to 
a combination of ENSO conditions and addi- 
tional favorable circumstances (Garreaud and 
Rutlland 1996; Vargas et al. 2000). In fact, all 
of the rainy events with a minimum amount of 
20 mm of rainfall that were recorded in the 
twentieth century in Antofagasta area occurred 
during El Nino years, while winter precipitation 
excesses were recorded in central Chile. How- 
ever, this relationship is conditioned by various 
other factors that control a northward shift of 
frontal systems and the spatial distribution of 
convective activity. During some El Nino years 



(even of strong intensity), it does not rain in 
northern Chile. 

In southern Peru, we showed that, at least at 
present, the relationship is much weaker be- 
tween strong rainfall episodes and ENSO con- 
ditions. First, a distinction must be made be- 
tween the coastal region and the area close to 
the cordillera. El Nino events are generally 
characterized by drought in the Altiplano and 
the Andean areas, while rainy episodes may or 
may not occur near the coast. As in northern 
Chile, the convective character of the rains may 
explain the apparently erratic location of the de- 
bris-flow activity, when it is observed. By ex- 
amining both the instrumental record and his- 
torical documentary data, we found that El 
Nino years are not characterized by precipita- 
tion excess (even in the coastal area). This is 
one difference from the situation observed in 
northern Chile. Another difference is that heavy 
rainfall episodes in coastal southern Peru may 
occur in different seasons. This observation 
suggests that different regional mechanisms 
may be involved, some of them possibly unre- 
lated to ENSO conditions. However, it does ap- 
pear that most debris-flow episodes in southern 
Peru over the past two centuries occurred dur- 
ing El Nino events. 

Before we address the question of the rela- 
tionship between late Pleistocene and early Ho- 
locene debris-flow activity and ENSO condi- 
tions, it may be useful to discuss how the geo- 
chronological framework for these kinds of de- 
posits was determined. 



Dating Debris-Flow Activity 

The scarcity of organic matter, plant remains, or 
material that can be dated within the debris-flow 
units generally hampers their direct age deter- 
mination. In only a few cases has it been ob- 
served that some mud flow overlaid or reworked 
charcoal remains and other remnants of human 
activity (shells, bones). In these cases, the radio- 
carbon age of the dated material provided a max- 
imum age for the debris-flow activity. In this 
study, we mentioned only geochronological data 
obtained on terrestrial material (plants, charcoal, 
and organic matter) and avoided data based on 
marine shells or bones of marine mammals. 
Large uncertainties about the reservoir effects, 
which may have varied over time in a region 
subject to various upwelling phenomena (Taylor 



46 



L. Ortlieb and G. Vargas 



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Debris-Flow Deposits and El Nino Impacts 



47 



and Berger 1967; Stuiver and Brazunias 1993; 
Southon et al. 1995), weigh upon radiocarbon 
results obtained on carbonates of marine origin. 
As Kennett et al. (2002) showed in a study based 
on a comparison of marine and terrestrial mate- 
rial from the Ilo region, it is not yet possible to 
determine whether the reservoir effect varied 
significantly since the late Pleistocene in this re- 
gion. The strong aridity so drastically limited the 
availability of fuel wood that the charcoal re- 
mains of archaeological sites may predate by 
several centuries the time of their ignition, thus 
impeding any calibration study between shells 
and charcoals. 

The radiocarbon ages measured on charcoal 
remains underlying debris-flow deposit are nec- 
essarily older than the rainfall episode that pro- 
voked the flow. But since the wood used for 
fire may have been burned several centuries af- 
ter the death of the tree, the apparent date of 
the charcoal may be significantly older than 
measured. These uncertainties must be kept in 
mind in the proposed comparison between max- 
imum ages of the debris-flow activity in the dif- 
ferent studied localities (Tables 3 and 4). How- 
ever, in spite of these unavoidable sources of 
unaccuracy, the general chronological frame- 
work proposed in Table 4 seems acceptable. 

Some of the dates measured on organic ma- 
terial (not charcoal) or roots within sedimentary 
units of the sequences at Quebrada Tacahuay 
and Los Burros by earlier authors may be more 
reliable because their contemporaneity with the 
deposits is better assessed. Two of this kind of 
radiocarbon result obtained in each quebrada 
(ca. 8660 and ca. 8970 cal. B.P.) compare rea- 
sonably well with the result obtained on the 
charcoal remains at a third locality (Playa 
Muerta, <9000 cal. B.P.) (Table 4). This obser- 
vation brings some confidence to the lateral cor- 
relation proposed here between the debris-flow 
remnants across the region. 

The stratigraphic disposition of the debris-flow 
units studied here, combined with the available 
geochronological data, thus indicate that a few ep- 
isodes of strong rainfall occurred before and im- 
mediately after the Pleistocene-Holocene bound- 
ary. It is inferred that violent rainfalls probably 
characterized this transition period. 

Because of the entrenchment of the hydro- 
graphic network starting in the middle Holo- 
cene, it is difficult to compare the frequency of 
occurrence of debris-flow activity throughout 
the Holocene. Once quebradas were subjected 



to vertical erosion, debris-flow deposits were 
less likely to be preserved on the interfluves, 
nor could they be recorded within the valleys. 
As a result, the limited number of late Holocene 
debris-flow units may be underestimated. Even 
with this restriction in mind, it seems clear that 
the debris-flow activity did not increase during 
the Holocene quite the contrary. In the local- 
ities visited in southern Peru, only one (or two) 
debris-flow deposits formed in the last thousand 
years was preserved, in sharp contrast to the 
tens of units recorded in Antofagasta Bay. The 
scarcity of recent debris-flow activity in the 
study area of southern Peru does not suggest a 
close relationship between ENSO conditions 
(known to have occurred with high frequency 
in the last few centuries) and the occurrence of 
strong rainfall events. 



Evidence for El Nino Conditions in the 
Latest Pleistocene-Early Holocene 

The occurrence of El Nino events and their char- 
acteristics (frequency, intensity) during the Early 
Holocene and at the end of the late Pleistocene 
is a much debated question (DeVries et al. 1997; 
Markgraf 1998; Sandweiss et al. 1999; Rodbell 
et al. 1999; Andrus et al. 2002; Bearez et al. 
2003). Keefer et al. (1998, 2001) developed the 
hypothesis that the presence of debris-flow de- 
posits along the coast of southern Peru consti- 
tuted evidence for El Nino conditions since be- 
fore the Late Glacial Maximum up to the pres- 
ent. On the other hand, Fontugne et al. (1999) 
argued that the lack of debris-flow units between 
8970 and 3380 cal. B.P. in Quebrada Los Burros 
could be interpreted as evidence for the lack of 
El Nino conditions between these two dates. 

In the case of Quebrada Los Burros, it can 
be objected that lack of a debris-flow record 
may be due to local geomorphic or hydrologic 
conditions and does not constitute a strong ar- 
gument against the occurrence of El Nino 
events. Anyway, debris-flow units from nearby 
localities (El Ahogado and Quebrada Tacahuay) 
provide evidence for the occurrence of local 
strong rainfall events in the middle Holocene 
and later. 

In Quebrada Tacahuay, debris-flow units and 
alluvial sediments interstratified in a thick sed- 
imentary sequence that encompasses the late 
Pleistocene and the first half of the Holocene 
suggest that the hydrologic conditions were 



48 



L. Ortlieb and G. Vargas 



quite different than at present. A thick alluvial 
sequence observed in Quebrada El Canon (Fig. 
8) supports the hypothesis that a high runoff 
existed at the end of the Pleistocene in the re- 
gion. A much wetter climate, with respect to 
the present-day situation, may thus have char- 
acterized the area between at least 13,000 cal. 
B.P. (or the Late Glacial Maximum?) and ca. 
9000 cal. B.P. If, as we suspect, this was true, 
then there is no reason to extrapolate the current 
(weak) relationship between ENSO and strong 
rainfalls. Local, relatively strong rainfalls may 
completely explain episodic debris-flow activity 
and the coarse alluvial deposits in several lo- 
calities of coastal southern Peru. 

Hence, we conclude that in coastal southern 
Peru, debris-flow activity is not straightfor- 
wardly related to ENSO conditions, even if in- 
strumental data for the last decades and docu- 
mentary historic data tend to suggest that some 
weak relationship may have existed recently. 
For more remote periods, during the postglacial 
late Pleistocene and early Holocene, the cli- 
matologic regime was quite different than at 
present. Until better knowledge of this regime 
is obtained, we believe it is misleading to infer 
a causal relationship between debris flow and 
ENSO in southern Peru for periods prior to the 
middle Pleistocene. 

Acknowledgments. This work was supported 
by the program Paleoclimatologie et Variabilite 
Climatique Tropicale (UR1), later replaced by 
the program Paleoenvironnements Tropicaux et 
Variabilite Climatique (PALEOTROPIQUE) of 
IRD. Fieldwork (November 1998) was aided by 
funding from the project Sud Perou (leader, D. 
Lavallee) within the program Paleoenvironne- 
ments et Evolution des Hominides (CNRS). 
Previous fieldwork was done while the senior 
author (and J. Machare) led a cooperative re- 
search project between ORSTOM (now IRD) 
and the Institute Geoffsico del Peru (1987- 
1991). G. Vargas (University of Chile) benefit- 
ed from an IRD scholarship while completing 
a doctoral thesis at the University of Bordeaux. 
We thank J. F. Saliege (LODYC, Universite de 
Paris-CNRS-IRD) for radiocarbon data on the 
localities of Tacahuay and El Ahogado, and J. 
Rutllant (University of Chile) for his useful 
comments on regional climate anomalies. We 
also thank Wilber Chambi (Universidad Jorge 
Basadre Grohmann, Tacna) for his help in com- 



piling newspaper-published regional data, and 
N. Guzman for her help in the field. 



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Paleoenvironment at Almejas: 

Early Exploitation of Estuarine Fauna 

on the North Coast of Peru 



Shelia Pozorski and Thomas Pozorski 



The preceramic site of Almejas, with radiocar- 
bon dates averaging about 5000 B.C.,' is among 
the earliest marine-oriented sites in the Casma 
Valley of Peru. The site consists of a dense shell 
midden over 1 m deep that is unusual because 
of the predominance of warm-water mud-flat 
mollusks among the remains. Along with these 
mollusks, an abundance of estuarine fishes in- 
dicates a very rich estuarine ecosystem close to 
the site. A single, well-preserved burial was also 
encountered within the shell midden. The collec- 
tive data from Almejas provide information 
about early coastal settlement that is pertinent to 
critical, much-debated issues regarding the tim- 
ing of current sea level attainment and the antiq- 
uity of the present climatic regime, including pe- 
riodic El Nino-related events. 



(Fig. 1). The site lies along the north side of a 
granite outcrop against which considerable gra- 
nitic sand is banked. Almejas is now about 5.5 
km from the Pacific Ocean and about 25 m 
above sea level, but the intervening area is quite 
low, less than 5 m above sea level (masl), and 
was once a large shallow estuary (Fig. 1). 

In the immediate vicinity of the site are abun- 
dant remains of much later Early Intermediate 
Period and Late Intermediate Period (200 B.C. 
to A.D. 1470) settlement, including a large cem- 
etery, cane foundations of quincha (wattle-and- 
daub) houses, and rich midden with abundant 
plant remains. Slightly further north, in a nat- 
ural basin also formed by low granitic hills, lies 
the Early Horizon site of San Diego (Pozorski 
and Pozorski 1987:51-65; Tello 1956:296-298; 
Thompson 1961:74-75, 241-244, 1964:208). 



The Site of Almejas 

Location and Surface Features 

A tiny preceramic site located near the aban- 
doned hacienda San Diego was named Almejas, 
a Spanish word meaning clam, because of the 
abundant bivalve shells found on the surface 



1 The 5000 B.C. date is based on uncalibrated radio- 
carbon dates. If calibrated dates were used, then the 
date for the site would be about 5900 B.C. However, 
for the purposes of this discussion, uncalibrated dates 
are used because the dates cited here for comparative 
purposes have been reported in the archaeological lit- 
erature as uncalibrated dates. 



Excavations at Almejas 

Almejas is distinguishable on the surface as an 
irregular patch of very dense shell about 95 m 
north-south by 50 m east-west. Excavation of 
four test pits within the area of dense shell re- 
vealed that this shell extends to a depth of 135 
cm. A 1-m 2 controlled stratigraphic excavation 
of the test pit exposed the deepest and best- 
preserved midden deposit. Portions of the upper 
levels had been disturbed and contaminated by 
the activities of later inhabitants. These mixed 
zones, which occasionally penetrated to a depth 
of 40 cm, were easily detected, both because of 
the extremely weathered condition of the early 



52 



Paleoenvironment at Almejas 



53 



2km 




Pacific 
Ocean 



Figure 1. Map of the lower Casma Valley showing the location of the site of Almejas. 



54 



S. Pozorski and T. Pozorski 




Figure 2. View from above showing three large boulders on top of the Almejas burial. 



shell and because of the presence of intrusive 
late elements such as ceramics, camelid dung, 
and maize. The lower levels, however, were un- 
disturbed and contained predominantly marine 
shell, fish bone, and wild plant remains. A buri- 
al was discovered within these intact lower lev- 
els. 

As the controlled stratigraphic excavation 
was carried out, excavation followed the visible 
stratigraphy. Thick levels were arbitrarily sub- 
divided into artificial levels 25 cm or less in 
thickness. Initial excavation of each level in- 
volved the removal of a 25-cm 2 column sample 
of midden that was screened through succes- 
sively smaller mesh: l /4 in. screen, a no. 10 geo- 
logical sieve, and a no. 25 geological sieve. The 
remaining material from the more general ex- 
cavation of each level was screened through a 
V* in. screen. The plant and animal remains re- 
covered when the column sample was screened 
through the % in. mesh were included as part 
of the general excavation material. Remains re- 
covered using the geological sieves were 
bagged separately according to mesh size. The 
animal bone recovered using the geological 
sieves was analyzed separately, but the results 
have been combined here under the term "col- 



umn sample." Volume measurements in liters 
were recorded for all excavation units within 
the stratigraphic cut. 



Burial 

A preceramic burial was encountered near the 
bottom of the stratigraphic excavation at a 
depth of 100 cm below the modern ground sur- 
face (Figs. 2 through 4). The first clue that a 
burial was present was three large boulders that 
lay on top of the burial wrapping (Fig. 2). This 
burial wrapping consisted of a well-preserved 
covering of parallel junco reeds (Cyperus sp.) 
laid lengthwise and closely spaced to cover the 
body (Fig. 3), but without any evidence of twin- 
ing or tying. 

The body (Fig. 4) was tightly flexed, lying 
on the right side with the head toward the north. 
The arms were flexed, bringing both hands into 
position beneath the chin. Based on examina- 
tion of the pelvis, the skeleton was determined 
to be that of a male. Formulae for stature cal- 
culations developed by Genoves (1967; repro- 
duced in Bass 1987:29) indicate that the man's 
stature when alive would have been approxi- 



Paleoenvironment at Almejas 



55 




Figure 3. View from above of the Almejas burial after removal of the three large boulders. Well-preserved loose 
junco (Cyperus sp.) fibers covered the exterior of the body. 



mately 161.5 cm. His age at death is estimated 
at approximately 35 to 45 years. This age de- 
termination is based on complete closure of all 
epiphyses (Bass 1987:13-19), slight arthritic 
lipping on the cervical vertebrae (Bass 1987: 
19), and tooth wear as measured against the 
scale developed by Brothwell (1981:72). All 
four third molars, the lower second premolars, 
and both lower right incisors were lost well be- 
fore death; their corresponding sockets are no 
longer visible. The remaining teeth are very 
worn, exposing the dentine. Both ears contain 
bony growths known as auditory exostoses; the 
condition is particularly severe in the left ear. 
These commonly result from trauma to the ear 
canal when the thin skin there is exposed to 
cold water while an individual is exploiting 
cold-water resources (Kennedy 1986; Quilter 
1989:21; Tattersall 1985:60-64; Wise et al. 
1994:217). 

A large quartz crystal (Figs. 4 and 5) was 
discovered near the left hand, where it may 
have been held. This item is unique in such a 
context; and, given the frequent inclusion of 
quartz crystals among power objects on the me- 
sas of modern shamans practicing on the Pe- 



ruvian north coast (Joralemon and Sharon 1993: 
20, 32, 54, 68, 80, 95, 107), the quartz crystal 
from Almejas may also have served prehistor- 
ically as a power object for communicating 
with and influencing the supernatural. This find 
represents the earliest such evidence of possible 
shamanistic practices along the entire central 
Andean coast. 

A total of 52 perforated shell discs were also 
collected from the grave fill between the junco 
wrapping and the center portion of the body 
(Fig. 5). These were likely strung as beads, pos- 
sibly once forming a necklace. Most of the shell 
discs were manufactured from Trachycardium 
procerum and Argopecten purpuratum shells, 
although a few may have been fashioned from 
the mussel Mytella guyanensis and the gastro- 
pod Thais chocolata. Shell beads and worked 
or cut shell ornaments have been found in some 
burials at Late Preceramic sites (Bird and Hys- 
lop 1985:66, 220; Feldman 1980:114, 121; 
Moseley 1992:1 16; Quilter 1 989:53-74 passim; 
Wendt 1976:34) and earlier preceramic sites 
(Stothert 1985:627). 

Other than the quartz crystal and shell discs 
associated with the burial, very few artifacts 



56 



S. Pozorski and T. Pozorski 




Figure 4. View from above of the excavated male skeleton at Almejas. The individual was 35 to 45 years old 
at the time of death and was buried with 52 perforated shell discs, which likely once formed a necklace, and a large 
quartz crystal, which he held in his left hand. 




Figure 5. Perforated shell discs and the large quartz crystal found with the Almejas burial. 



Paleoenvironment at Almejas 



57 



TABLE 1. Radiocarbon dates from Almejas. 



Sample no. 


Radiocarbon 
years* B.C. 


B.C. 

equivalents 


Calibrated 
datet 


Material 


Context 


UGa-4518 


7195 


75 


5245 


75 


5980 


130 


Charcoal 


Stratigraphic cut, level 4c, 
80 cm below surface 


UGa-4519 


7220 


70 


5270 


70 


6000 


120 


Charcoal 


Stratigraphic cut, level 4e, 
100 cm below surface 


UGa-4539 


6875 


105 


4925 


105 


5675 


180 


Junco 


From burial fiber wrapping, 
burial cut into level 4e 



* All dates are based on the Libby half-life (5568 30 years) and have no "C/ I2 C corrections. 
t Calibrations are based on charts in Stuiver and Becker (1993). 



were encountered at Almejas. These additional 
artifacts include rounded shell discs and perfo- 
rated pieces of shell that may represent partially 
shaped perforated shell discs or beads. 

The burial at Almejas is one of the earliest 
preceramic burials that have been found along 
the central Andean coast. Dating to approxi- 
mately 5000 B.C., this burial predates all burials 
associated with the Late Preceramic Period or 
the Cotton Preceramic Period (3000-1800 B.C.), 
a time period associated with the use of twined 
cotton textiles for clothing, burial wrappings, 
and netting (Bird and Hyslop 1985:64-76; Lan- 
ning 1967:61: Moseley 1983:208, 1992:108- 
109). A few widely scattered coastal sites have 
yielded burials of comparable age: the earliest 
burials at La Paloma on the central Peruvian 
coast (Quilter 1989:11, 163-165), the burials 
associated with the Late Las Vegas phase at the 
Las Vegas in southern Ecuador (Stothert 1985: 
618-619), and those of the Chinchorro Culture 
in northern Chile and the far south coast of Peru 
(Arriaza 1995:127-130). Somewhat earlier 
burials (6000-8000 B.C.) have been found with- 
in the Chinchorro culture sites (Arriaza 1995: 
126-127), at Encampment 96 of Paracas Bay 
(Arriaza 1995:55; Engel 1981:31-32; Quilter 
1989:71), at the Paijan culture sites of Quiri- 
huac Shelter in the Moche Valley (Chauchat 
1988:49-51; Moseley 1992:87), and in the 
Cupisnique desert north of the Chicama Valley 
(Chauchat 1978b:60, 1988:59-63). 

The Almejas burial has several traits typical 
of and other traits not so characteristic of pre- 
ceramic burials along the central Andean coast. 
The body itself was buried in its natural state 
with no attempt at artificial mummification. 
With the exception of the unique Chinchorro 
Culture (Arriaza 1995), this was standard treat- 
ment for all preceramic burials along the coast. 
The flexed position of the Almejas body, lying 



on one side, is typical of many preceramic sites, 
including those contemporary with, earlier than, 
and later than the Almejas burial (Bird and 
Hyslop 1985:64-76; Engel 1981:32-38; Feld- 
man 1980:114-122; Grieder et al. 1988:Table 
4; Moseley 1992:116; Pozorski and Pozorski 
1979:351-354, 1987:20; Quilter 1989:53; 
Stothert 1985:625; Wendt 1976:29-30; Wise et 
al. 1994:215). The presence of large stones on 
top of the Almejas burial is also a trait shared 
with burials at several preceramic sites (Bird 
and Hyslop 1985:66; Pozorski and Pozorski 
1979:353, 1987:20: Quilter 1989:83; Stothert 
1985:625; Wendt 1976:30). The wrapping of 
bodies was a widespread practice in preceramic 
times. In Late Preceramic times, cotton cloth 
was most frequently used (Bird and Hyslop 
1985:64-76; Feldman 1980:114-122; Moseley 
1992:1 16); also common was the use of twined 
or woven matting (Bird and Hyslop 1985:66- 
74; Engel 1976:97, 1981:32-38; Feldman 1980: 
114-118; Fung Pineda 1988:95; Quilter 1989: 
53, 70-82; Wendt 1976:30-31). The use of 
loose junco fibers, totora reeds, or other loose 
plant fiber as a burial wrapping was less com- 
mon (Bird and Hyslop 1985:74; Pozorski and 
Pozorski 1987:20; Quilter 1989:87-162). 



Subsistence and Environment 

Two features of Almejas distinguish the site 
from other preceramic sites of the central and 
north coast. First, the radiocarbon dates for the 
site, averaging about 5000 B.C. (Table 1), are 
unusually early. Second, the predominant fau- 
nal remains argue for a nutrient-rich estuary in 
the vicinity of the site. The molluscan inventory 
is dominated by species that disappeared from 
the Casma area quite early and are now largely 



58 



S. Pozorski and T. Pozorski 

Percentage of Shellfish Species Based on MNI 



KV^ 



.^ 



Level 












la 

1b 
2a 
2b 
3a 
3b 
4a 
4b 
4c 
4d 
4e 
5 

Figure 6. 

Individuals). 






a 



E3 

Y777A WA 









Y/////////////A 

X//////////7777A 

Y/////////////A 

Y/////////777A 



V///////A 
V///////X 







VTA 








I I 



I I 



I I 
I I 



I I 
I I 



V///7//A 

Y////////S77\ 

Y///////A 

Diagram of shellfish species frequency through time at Almejas, based on MNI (Minimum Number of 
Level 5 is the earliest level; level la is the latest. 



confined to mud-rich substrate habitats within 
warmer waters much farther north, near the 
modern Peru-Ecuador border and beyond. Fish 
species identified at Almejas also argue for the 
presence of a local warm-water estuarine envi- 
ronment with one or more inlets that afforded 
access to the cooler offshore waters. 



Subsistence 

Although marine mollusks and fish were the 
main food source, there is some evidence of 
plant food use. Fragments of gourd rind (La- 
genaria sicerarid) were found in the middle 
levels of the cut, well below any evidence of 
disturbance or contamination. Immature fruits 
of this plant may have been used as food, and 
the presence of rind fragments points to the use 
of gourd containers. Other than gourd, only re- 
mains of wild plants were recovered from the 
preceramic midden. The dominant species was 
algarrobo (Prosopis chilensis). Seeds of this 
plant were very common, suggesting that the 



sweet bean pods, readily available from trees 
on the valley edges, were a source of food. 

Warm-blooded vertebrates, including birds 
and marine and terrestrial mammals, composed 
an additional, relatively minor food source. 
Bones of rails (Rallidae), cormorants (Phala- 
crocorax spp.), mice (Cricetinae), sea lion 
(Otariidai), and deer were identified among the 
faunal remains within the stratigraphic excava- 
tion (Reitz 1995b). However, none except the 
mouse species is represented by more than one 
or two bones. 

The molluscan species inventory of Almejas 
is unusual because it is dominated by shellfish 
species, which favor the muddy, silt-rich sub- 
strate typical of estuaries and are now available 
almost exclusively in the warm-tropical waters 
of the far north coast of Peru (Figs. 6 through 
10). These include Chione subrugosa (Figs. 6 
through 8), the most common species at Al- 
mejas, as well as substantial numbers of Mytella 
guyanensis (Figs. 6, 7, and 9), Mytella arcifor- 
mis (Figs. 6, 7, and 10), Protothaca asperrima, 
and Trachycardium procerum, and, more rarely, 



Paleoenvironment at Almejas 

Percentage of Shellfish Species by Weight 



59 



Leve, 



" 









la 

1b 
2a 
2b 
3a 
3b 
4a 
4b 
4c 
4d 
4e 
5 





B 






Y7777\ 
V77A 



I 

I 













VTA 



Y/////////X 
Y777A 







Y/////////7777)( 
Y/////////7777A 
Y/////////7777\ 
V////////////A 



V////////A 

V//////X 

V///////X 

V///////A 



Q 




D 



I 



I I 



I Q I I 
B I B 



I I 




B 





I I 

i i o e 

I I B B 

I I Q B 

I I fl 



Q 



Figure 7. Diagram of shellfish species frequency through time at Almejas based on weight of sample. Level 5 
is the earliest level; level la is the latest. 



Mactra fonsecana, Nassarius luteostoma, Cer- 
ithium stercusmuscarum, and Cerithidea albon- 
odosa (Figs. 6 and 7) (Keen 1 97 1:63-6 10 pas- 
sim; Olsson 1961:113-325 passim). Even 
slightly later local preceramic and early ceramic 
middens contain few to none of these species, 
which suggests that they disappeared from the 
area quite early. Not all shellfish from Almejas 
are species that inhabit exclusively a mud flat 
habitat. Tagelus dombeii (Figs. 6 and 7) is 
known to occur in sandy substrates (Coker, cit- 
ed in Dahl 1909:160), and this species has a 
known range that extends northward to Panama 
and southward to Chile (Dall 1909:160; Keen 
1971:246; Olsson 1961:351). Also significantly, 
shellfish typical of warm-temperate waters are 
represented by a number of chiton plates and 
shells of Tegula atra, Brachidontes purpuratus, 
Thais chocolata, Choromytilus chorus, and lim- 
pets (Figs. 6 and 7). These species characteristic 
of colder water were accessible in the rocky 
areas washed by open surf near the modern 
town of Puerto Casma. They were much more 
frequently exploited later, and came to domi- 



nate the faunal inventory of sites established in 
the area after the silting in and eventual desic- 
cation of the estuary near Almejas. Clearly, the 
inhabitants of Almejas placed much greater em- 
phasis on the abundant and more readily acces- 
sible shellfish within the local estuary, a rich 
microenvironment teeming with plant and ani- 
mal life. 

The medium to large bivalve shells from Al- 
mejas exhibit consistent fracture patterns (Figs. 
8 to 1 0), which indicates they were bashed open 
with a simple pounding tool. Because cooked 
shellfish are easily opened, it seems most likely 
that the inhabitants of Almejas consumed local 
mollusks raw. 

Fish species consumed by the inhabitants of 
Almejas also reflect the site's proximity to the 
resource-rich local estuarine environment. Bar- 
rier islands protect such environments from the 
ocean, promoting the deposition of the fine riv- 
er-borne sediments that compose the component 
mud flats and facilitate the formation of marsh- 
es (Odum 1971:352-362). Nevertheless, estu- 
aries experience tidal fluctuations through open- 



60 



5. Pozorski and T. Pozorski 




Figure. 8. Whole and fragmentary specimens of Chione subrugosa showing the characteristic breakage pattern 
evincing live shellfish consumption. 



MET( ? 1C 'I , 21 , 31 , 4, , 5, . 61 . 71 8 




Figure 9. Fragmentary specimens of Mytella guyanensis showing the characteristic breakage pattern evincing 
live shellfish consumption. 



Paleoenvironment at Almejas 



61 




Figure 10. Whole and fragmentary specimens of Mytella arciformis showing the characteristic breakage pattern 
evincing live shellfish consumption. 



ings that connect the estuary with a nearby bay 
or open ocean (Odum 1971; Reitz 1995b). The 
resulting environment is dynamic and much 
more productive than offshore waters because 
nutrients tend to be trapped and concentrated 
there, and photosynthesis occurs throughout the 
year (Odum 1971). Especially relevant to the 
Casma situation is the fact that estuaries func- 
tion as nurseries for many organisms, including 
fish, thereby increasing their natural richness 
(Odum 1971:356). Adult fish may spawn in the 
ocean, with the larvae being carried into the 
estuary by tidal currents. Other adult fish may 
enter the estuaries to spawn, with their young 
remaining there until they reach maturity. Adult 
fish may spend more or less time within estu- 
aries. They are attracted by the rich biomass as 
a food source, yet temporarily intolerable tem- 
peratures or salinity may induce them to leave 
the estuarine ecosystem for more stable off- 
shore water (Reitz 1995b; Hackner et al. 1976, 
cited in Reitz 1995b). Other species that fre- 
quent shallow near-shore waters may be attract- 
ed to the vicinity of estuary inlets and even into 
the estuary because of the richer food supply 
available in such zones. 



Since the estuary near Almejas was such a 
critical part of the ecosystem which supported 
the site's inhabitants, it is important to assess 
the fish species relative to their potential role 
within this feature of the local environment. To 
accomplish this, we used Reitz's (1995b) ex- 
cellent review and synthesis of the available 
habitat data for the fish species identified from 
Almejas, which draws primarily on Chirichigno 
(1974, 1982) and Schweigger ( 1 964) as well as 
additional sources (DEIS 1978; Hoese and 
Moore 1977; Moreno and Castilla n.d. all cit- 
ed in Reitz 1995b). The results are presented in 
Tables 2 through 4. These tables reveal that fish 
species consumed at Almejas fall into three 
principal groups: species that frequent estuaries, 
species native to the warm-temperate waters of 
the Peruvian Current, and mixed-habitat species 
that are known to inhabit both warm-temperate 
and warm-tropical waters. Significantly, only 
three species that are more typical of warm- 
tropical waters were identified among the fauna! 
remains. Several estuarine species were initially 
classified as warm-tropical species (Reitz 
1995b); however, assessment of fish habitat 
data in light of the reconstructed local estuarine 



62 



S. Pozorski and T. Pozorski 



TABLE 2. Fish species identified from the column sample. 



MNI 




Biomass* 










Weight, 






Species 


NISP 


No. 


(%) 


g 


kg 


(%) 


Estuarine fish species 














Elops affinis (ladyfish) 


9 


2 


(1.54) 


0.039 


0.0122 


(1-79) 


Clupeidae (herrings) 


806 


38 


(29.23) 


6.639 


0.1713 


(25.18) 


Engraulidae (anchovies) 


4,809 


67 


(51.54) 


8.840 


0.2142 


(31.49) 


Ariidae (sea catfishes) 


4 


3 


(2.31) 


0.140 


0.0032 


(0.47) 


Bairdiella spp. (silver perch) 


1 


1 


(0.77) 


0.030 


0.0029 


(0.43) 


Mugil spp. (mullet, lisa) 


105 


9 


(6.92) 


1.128 


0.0322 


(4.73) 


Subtotal 




120 


(92.31) 




0.4360 


(64.09) 


Warm-temperate fish species 














Myliobatidae (eagle rays) 


4 


2 


(1.54) 


0.110 


0.0198 


(2.91) 


Sciaena spp. (lorna) 


3 


3 


(2.31) 


0.028 


0.0037 


(0.54) 


Subtotal 




5 


(3.85) 




0.0235 


(3.45) 


Mixed-habitat fish species 














Elasmobranchiomorphi 














(cartilaginous fishes) 


1 


1 


(0.77) 


0.009 


0.0022 


(0.32) 


Dasyatidae (stingrays) 


3 


1 


(0.77) 


0.070 


0.0128 


(1.88) 


Muraenidae (morays) 


1 


1 


(0.77) 


0.010 


0.0008 


(0.12) 


Cynoscion spp. (seatrout) 


1 


1 


(0.77) 


0.020 


0.0022 


(0.32) 


Subtotal 




4 


(3.08) 




0.0180 


(2.64) 


Warm-tropical fish species 














Gerridae (Mojarras) 


1 


1 


(0.77) 


0.009 


0.0006 


(0.09) 


Subtotal 




1 


(0.77) 




0.0006 


(0.09) 


Unidentified fish 


849 






8.340 


0.2022 


(29.72) 



Abbreviations: NISP, number of identified species; MNI, minimum number of individuals. 

* Biomass values are based on calculations made by Reitz (1995b; Reitz and Cordier 1983; Reitz et al. 1987). 



environment led the authors to conclude that 
virtually all of these species should more ap- 
propriately be viewed as estuary dwellers. The 
differences between the fish species identified 
from the column sample as compared to the 
general excavation (Tables 2 and 3) are partic- 
ularly noteworthy in this regard. The fish re- 
mains from the column sample (no. 10 and no. 
25 geological sieves) strongly reflect exploita- 
tion of the estuary, where small fishes, both 
young fishes and small adult fishes, could be 
easily taken. The small herrings and anchovies 
are included in Table 2 as estuarine fish because 
some species within both families are known to 
frequent estuaries and because their consistent, 
small size within the archaeological sample 
suggests that the estuary served as their nurs- 
ery. In contrast, adults of these two species are 
known to frequent the offshore waters of the 
Peruvian Current; therefore, the herring and an- 



chovy remains recovered from the general ex- 
cavation (V4 in. screen) were included among 
the warm-temperate fish in Table 3. Tables 2 
and 3 also reveal the paramount importance of 
the estuary as a food source. More than 64% of 
the fish biomass reconstructed for the column 
sample came from estuarine fishes, versus 
3.45% for the warm-temperate fishes and 
2.64% for the mixed-habitat fishes (Table 2). 
More balance can be seen with respect to the 
fish biomass reconstructed for the general ex- 
cavation, with almost 24% comprised of estu- 
arine species, over 21% comprised of warm- 
temperate species, and over 14% comprised of 
mixed-habitat fish (Table 3). These proportions 
are in keeping with the reconstructed subsis- 
tence scenario. Adult mullet and sea catfish are 
known to inhabit estuaries and have been clas- 
sified accordingly. The other adult species rep- 
resented by vertebrate remains from the general 



Paleoenvironment at Almejas 



63 



TABLE 3. Fish species identified from the general excavation. 



MNI 




Biomass* 










Weight, 






Species 


NISP 


No. 


(%) 


g 


kg 


(%) 


Estuarine fish species 














Albula vulpes (bonefish) 


1 


1 


(0.97) 


0.080 


0.0041 


(0.10) 


Ariidae (sea catfishes) 


220 


21 


(20.39) 


39.170 


0.6858 


(17.26) 


Micropogonias spp. (croaker) 


9 


5 


(4.85) 


2.760 


0.0949 


(2.39) 


Mugil spp. (mullet, lisa) 


114 


15 


(14.56) 


8.000 


0.1665 


(4.19) 


Subtotal 




42 


(40.77) 


50.010 


0.5913 


(23.94) 


Warm-temperate fish species 














Myliobatidae (eagle rays) 


1 


1 


(0.97) 


0.430 


0.0609 


(1.53) 


Clupeidae (herrings) 


150 


11 


(10.68) 


4.669 


0.1089 


(2.74) 


Engraulidae (anchovies) 


9 


4 


(3.88) 


0.168 


0.0081 


(0.20) 


Pamlabrax spp. (cabrilla) 


7 


4 


(3.88) 


0.560 


0.0094 


(0.24) 


Trachurus murphvi 














(jack mackerel, jurel) 


9 


4 


(3.88) 


2.350 


0.0885 


(2.23) 


Anisotremus spp. (sargo) 


1 


1 


(0.97) 


0.080 


0.0030 


(0.08) 


Sciaenidae (drums) 


5 






0.760 


0.0318 


(0.80) 


Paralonchurus spp. (coco) 


28 


5 


(4.85) 


9.080 


0.2642 


(6.65) 


Sciaena spp. (lorna) 


24 


8 


(7.77) 


1 1 .260 


0.2421 


(6.09) 


Bodianus spp. (hogfish) 


1 


1 


(0.97) 


0.270 


0.0093 


(0.23) 


Sarda spp. (bonito) 


3 


1 


(0.97) 


0.790 


0.0226 


(0.57) 


Subtotal 




40 


(38.83) 


30.417 


0.8488 


(21.36) 


Mixed habitat fish species 














Carcharhinidae (requiem sharks) 


11 


3 


(2.91) 


1.360 


0.1864 


(4.69) 


Dasyatidae (stingrays) 


9 


3 


(2.91) 


1.720 


0.2249 


(5.66) 


Muraenidae (morays) 


1 


1 


(0.97) 


0.030 


0.0019 


(0.05) 


Serranidae (sea basses) 


2 






0.200 


0.0033 


(0.08) 


Carangidae (jacks) 


1 






0.130 


0.0065 


(0.16) 


Trachinotus spp. (pompano) 


1 


1 


(0.97) 


0.050 


0.0028 


(0.07) 


Cynoscion spp. (seatrout) 


13 


6 


(5.83) 


1.620 


0.0759 


(1.91) 


Bothidae (flounders) 


6 


3 


(2.91) 


2.520 


0.0639 


(1.61) 


Subtotal 




17 


(16.50) 


7.630 


0.5656 


(14.24) 


Warm-tropical fish species 














Epinephelus spp. (grouper) 


12 


3 


(2.91) 


2.630 


0.0522 


(1.31) 


Gerridae (Mojarras) 


3 


1 


(0.97) 


0.210 


0.0075 


(0.19) 


Subtotal 




4 


(3.88) 


2.840 


0.0597 


(1.50) 


Unidentified fish 


1,810 






1 1 1 .900 


1.5473 


38.95 



Abbreviations: NISP, number of identified species; MNI, minimum number of individuals. 

* Biomass values are based on calculations made by Reitz (1995; Reitz and Cordier 1983; Reitz et al. 1987). 



excavation are potential offshore species that 
may have been taken in the cooler waters of the 
open ocean, near estuary inlets because of the 
richer nutrients, or even within the estuary 
the richest of the three potential environments. 
This is especially likely for sargo (Anisotremus 
spp.), seatrout (Cynoscion spp.), coco (Paralon- 
churus spp.), lorna (Sciaena spp.), flounders 
(Bothidae family), and members of the jack 
family (Carangidae), all of which are known to 
inhabit shallow inshore waters. 



Environment 

The archaeological data from Almejas must be 
viewed in relation to three radiocarbon dates 
from its midden: 5245 75 B.C. (UGa-4518), 
5270 70 B.C. (UGa-4519), and 4925 105 
B.C. (UGa-4539) (Table 1 ). These dates cluster 
around 5000 B.C. (uncalibrated). Several other 
sites along the western coast of South America 
are known to date as early as Almejas or earlier. 
The earliest coastal sites that show heavy reli- 



64 



S. Pozorski and T. Pozorski 



TABLE 4. Combined biomass values for fish species identified at Almejas.* 



Estuarine fish 
species 



Warm-temperate 
fish species 



Mixed-habitat 
fish species 



Warm-tropical 
fish species 



Unidentified 
fishes 



Sample 



kg 



kg 



kg 



kg 



kg 



General excavation 


0.9513 


(23.94) 


0.8488 


(21.36) 


0.5656 


(14.24) 


0.0597 


(1.50) 


1.5473 


(38.95) 


Column 


sample 


0.4360 


(64.09) 


0.0235 


(3.45) 


0.0180 


(2.64) 


0.0006 


(0.09) 


0.2022 


(29.72) 


Adjusted 


columnt 


5.7988 


(64.09) 


0.3125 


(3.45) 


0.2394 


(2.64) 


0.0080 


(0.09) 


2.6893 


(29.72) 



Total 



6.7501 (51.84) 1.1613 (8.92) 0.8050 (6.18) 0.0677 (0.52) 4.2366 (32.54) 



* Biomass values are based on calculations made by Reitz (1995b; Reitz and Cordier 1983; Reitz et al. 1987). 
t The column sample values were adjusted upward based on the proportion that the column sample volume (109 
liters) represented of the total volume of the stratigraphic excavation (1,454 liters), resulting in a factor of 13.3. 



ance on marine resources are known from the 
far north of Peru near Talara (Richardson 1978, 
1981), in southern Ecuador (Stothert 1985), 
from far southern Peru near Ilo (Sandweiss et 
al. 1989), and from northern Chile near Anto- 
fagasta (Aldenderfer 1989:117-144; Llagostera 
Martinez 1979; Richardson 1981, 1994:38-39). 
These sites tend to be located where the conti- 
nental shelf is narrow, thereby minimizing the 
impact of the subsequent shoreline transgres- 
sion believed to have inundated ancient shore- 
line sites where the shelf is wide (Richardson 
1981). These sites also tend to have faunal re- 
mains consistent with their geographic location. 

Three additional sites or site complexes are 
more comparable to Almejas based on their ra- 
diocarbon dates and because of the presence of 
what have been described as thermally anoma- 
lous fish and/or shellfish species. These include 
the Paijan complex sites, located well inland 
between the Chicama and Jequetepeque Val- 
leys, which have been dated to approximately 
8550-6050 B.C. (Chauchat 1988; Reitz 1995a, 
1995b), as well as Ostra Base Camp and Pampa 
las Salinas, located north of the Santa River 
mouth, with radiocarbon dates of ca. 6000 B.C. 
(Reitz 1995a, 1995b, 2001; Sandweiss et al. 
1983, 1986, 1996). 

The data from Almejas are especially rele- 
vant to the controversial issues of when the sea 
level attained its present level and the antiquity 
of the present climatic regime and its associated 
current patterns (DeVries and Wells 1990; 
DeVries et al. 1997; Kerr 1999; Rodbell et al. 
1999; Rollins et al. 1986, 1997; Sandweiss 
1986; Sandweiss et al. 1983, 1996, 1997, 1998, 
1999; Wells 1988:160-176; Wells and Noller 
1997). The authors' reconstruction of the en- 
vironment of Almejas at the time of its occu- 



pation suggests that the sea level and climatic 
conditions in effect today are in fact quite old. 

The warm-temperate water of the Peruvian 
Current was likely present off the Casma Valley 
coast at least by about 7000 years ago, when 
Almejas was occupied. Arguments for consid- 
erable antiquity for the current climatic regime 
are based on the faunal inventory of Almejas, 
subsistence activities practiced at the site, and 
preservation within the site. Both fish and shell- 
fish species provide evidence that cold water 
was readily accessible from the site. Additional 
evidence that these species characteristic of 
warm-temperate water were taken by the inhab- 
itants of Almejas comes from the human skel- 
eton, which was characterized by auditory ex- 
ostoses, bony growths that develop in the ear 
canal as a result of repeated exposure to cold 
water (Kennedy 1986). Finally, the preservation 
of fragile plant material including the junco 
burial wrapping, gourd rind, and algarrobo 
seeds within the Almejas midden argues for a 
near-rainless climate of the type that exists to- 
day. Without the Peruvian Current offshore, the 
climate would have been significantly wetter, 
and preservation would have been negatively 
affected. 

Sea level was probably close to or slightly 
higher than current levels at the time Almejas 
was in use (Wells 1988:161-162). Evidence for 
this comes from the fact that an estuary was 
present at the mouth of the Casma River at this 
time (Wells 1988:161-162). Formation of this 
estuary depended on the sea level being at or 
slightly above its present height. Ample evi- 
dence for the existence and exploitation of this 
rich estuarine environment comes from the 
many warm-water mud flat molluscan species 
and the estuarine fish species, especially the im- 



Paleoenvlronment at Almejas 



65 



mature individuals recovered through fine 
screening, that make the Almejas faunal inven- 
tory so remarkable. These species most likely 
became established in the estuarine environ- 
ment when free-floating or free-swimming mol- 
luscan larvae and fish traveled south within the 
warm Ecuadorian Countercurrent during an in- 
frequent El Nino event. They would have 
thrived within the shallow, nutrient-rich, sun- 
warmed estuarine environment (DeVries and 
Wells 1990; Smith 1944:v). The Casma Valley 
is an especially favorable place for this to occur 
because of the large number of sunny days 
(ONERN 1972:50). 

Warm-temperate species were available on 
the rocky headlands and slightly offshore, but 
mud flat estuarine species were clearly pre- 
ferred. This preference probably reflects both 
their abundance in the rich estuarine habitat and 
their ease of capture, especially for people who 
apparently lacked a well-developed fishing 
technology. Nutrients from the estuarine envi- 
ronment would have spilled out into the ocean, 
thereby attracting warm-temperate fish and 
making them more accessible to the people of 
Almejas. 

Ironically, the same sea level rise or trans- 
gression that initially facilitated development of 
the estuarine environment that likely attracted 
the inhabitants of Almejas to settle nearby also 
triggered deposition of river-borne sediments 
(DeVries and Wells 1990; Wells 1988:172- 
176). Gradual filling by these sediments ulti- 
mately eliminated the estuary a local environ- 
mental change that also likely led to the aban- 
donment of Almejas. Similar sequences of es- 
tuary development and backfilling by 
river-borne sediment likely occurred in other 
coastal areas, thereby also explaining occasion- 
al occurrences of colonies of tropical fauna of 
relatively long duration within an otherwise 
temperate zone. This would also explain why 
estuaries were once more common, but are now 
rare. 

Variation in the frequency of specific shell- 
fish species through time may be correlated 
with the gradual silting in of the estuarine en- 
vironment that eventually led to its disappear- 
ance and the abandonment of Almejas. The 
charts in Figures 6 and 7 clearly reveal that six 
species comprise most of the molluscan inven- 
tory: Mytella arciformis, Protothaca asperima, 
Mytella guayanensis, Chione subrugosa, Tage- 
lus dombeii, and Trachycardium procerum, 



with the latter showing a significant presence 
more clearly in Figure 7. It is also readily ap- 
parent that Mytella arciformis dominates the 
shellfish inventory in the earliest levels and that 
Protothaca asperima and Mytella guayanensis 
exhibit their greatest frequencies of occurrence 
slightly later within the stratigraphic sequence. 
Tagelus dombeii peaks in frequency even later 
in the sequence, whereas Chione subrugosa, the 
most abundant mollusk overall, exhibits its 
highest frequency toward the end of the strati- 
graphic sequence. 

Habitat data are rarely supplied in great de- 
tail, but the data available for the principal spe- 
cies indicate that two of the three species that 
predominate in the early and early-middle por- 
tion of the sequence are known to occur in con- 
siderably deeper water than most species that 
predominate in the late and middle-late portion 
of the sequence. Specifically, the habitat of My- 
tella arciformis has been described as "six fath- 
oms, mud" (Hertlein and Strong 1946:72), and 
Prothaca asperrima has been described as oc- 
curring "in sandy mud at a depth of 13 fath- 
oms" (Hertlein and Strong 1946:187). When 
specific depth measurements are provided for 
one species with peak frequencies toward the 
latter part of the sequence, the habitat depth is 
much shallower. Live specimens of Tagelus 
dombeii are described as being "taken in sand 
under three or four feet of water" (Coker, quot- 
ed in Dahl 1909:160). However, live individuals 
of Trachycardium procerum, which are slightly 
more abundant during the latter portion of the 
sequence, were "found in coarse sand in from 
four to six fathoms of water" (Sowerby 1833: 
83), and each of the six dominant species has 
been described by one or more experts as oc- 
curring in shallow water, lagoons, shallow la- 
goons, on mud flats, at low water, and in inter- 
tidal zones, indicating that all could be found 
at times in relatively shallow water (Hertlein 
and Strong 1946:72-191 passim; Keen 1971: 
63-246 passim; Olsson 1961:298; Soot-Ryen 
1955:53, 55; Sowerby 1835:41). 

When the available data on the geographic 
distribution of the principal species are consid- 
ered, the three species with peak frequencies 
earlier in the sequence appear more narrowly 
confined to warm-tropical zones. Mytella arci- 
formis is known from El Salvador to Ecuador 
or Peru (Hertlein and Strong 1946:72; Keen 
1971:63), Mytella guayanensis is known from 
Mexico or the Gulf of California to northern 



66 



S. Pozorski and T. Pozorski 



Peru (Hertlein and Strong 1946:72-73; Keen 
1971:63; Soot-Ryen 1955:53, 55), and Proto- 
thaca asperrima is known from California to 
Peru more commonly northern Peru (Dahl 
1909:158; Hertlein and Strong 1946:187; Keen 
1971:193). In contrast, Tagelus dombeii is 
known from Panama to Chile (Dahl 1909:160; 
Keen 1971:246; Olsson 1961:351); Chione sub- 
rugosa is described by Dahl (1909:158) as oc- 
curring from the Gulf of California to Valpa- 
raiso, Chile (although other experts describe a 
more northern range, from the Gulf of Califor- 
nia to Peru: Hertlein and Strong 1946; Keen 
1971:190; Olsson 1961:298); and Trachycar- 
dium procerum is known from the Gulf of Cal- 
ifornia to northern Chile or Chile (Keen 1971: 
155; Olsson 1961:247-248). These data likely 
reflect the greater tolerance of Chione subru- 
gosa, and especially Tagelus dombeii and Tra- 
chycardium procerum, to more varied environ- 
ments, including cooler water. This may have 
allowed these species to survive as the estuary 
filled with silt, became smaller in area, and was 
likely more impacted by the cooler water of the 
adjacent open ocean at its outlet. Such an in- 
terpretation might also explain the relatively 
rare but continued presence of remains of these 
three species at later preceramic and Initial Pe- 
riod (1800-900 B.C.) sites. 



Discussion and Conclusions 

As a result of recent fieldwork and research, 
other archaeological sites similar to Almejas 
have been discovered that date quite early with- 
in the Andean sequence and have yielded faunal 
assemblages that reflect the presence of species 
not currently typical of their respective lati- 
tudes. These include the Paijan complex sites 
north of the Chicama Valley and the sites of 
Pampa las Salinas and Ostra Base Camp north 
of the Santa River mouth (Andrus et al. 2002; 
Chauchat 1976, 1978, 1988; Reitz 1995a, 
1995b, 2001; Rollins et al. 1986; Sandweiss et 
al. 1983, 1996). 

Initially, the sites north of Santa attracted at- 
tention because of the presence of shellfish cur- 
rently known to inhabit warm-tropical waters 
(Rollins et al. 1986; Sandweiss et al. 1983), as 
did the site of Almejas. These data from the 
Santa sites in particular were initially used to 
argue for the continuous presence of warmer 



currents much further south, an absence of 
ENSO events, and a corresponding wetter cli- 
matic regime much different from today's cli- 
mate (Rollins et al. 1986; Sandweiss et al. 
1983). As additional faunal material was ana- 
lyzed from the Paijan complex sites, from the 
Santa area, and from Almejas in Casma, fish 
species were identified that are not currently 
typical of these areas. These results have been 
used by many of the same investigators as fur- 
ther evidence of the presence of warmer off- 
shore waters (Andrus et al. 2002; Reitz 1995a, 
1995b, 2001; Sandweiss et al. 1996). 

An alternative scenario maintains that the 
current climatic regime, including periodic 
ENSO events, is quite ancient. Indeed, evidence 
from the far south coast site of Quebrada Ta- 
cahuay indicates that ENSO events were pre- 
sent at least as early as the late Pleistocene 
(Keefer et al. 1998). The seemingly out-of- 
place species represent colonies of thermally 
anomalous fauna whose larvae were carried 
southward within the warm currents of a peri- 
odic ENSO event (S. Pozorski and T. Pozorski 
1995; DeVries et al. 1997; Wells and Noller 
1997). As the sea level rose to approximately 
modern limits, estuaries formed at the mouths 
of some rivers, and the resultant shallow, sun- 
warmed, nutrient-rich waters readily supported 
species adapted to warmer estuarine waters 
(DeVries et al. 1997; DeVries and Wells 1990; 
Wells and Noller 1997). Also according to this 
scenario, ENSO events were essential to stock 
the estuaries with appropriate fish and shellfish 
species, after which time the cooler offshore 
Peruvian Current would have returned. Once in- 
troduced, these warm-tropical shellfish and fish 
species would have flourished in these estuaries 
as long as local environmental conditions re- 
mained favorable. Subsequent ENSO events 
could potentially have introduced additional 
shellfish and fish species, but such events were 
not essential for the survival of these species in 
their localized estuarine environments. Hence, 
fluctuations in the periodicity of ENSO events 
are not especially relevant with respect to the 
survival of these thermally anomalous shellfish- 
es and fishes in estuarine conditions. The criti- 
cal variable was the maintenance of local en- 
vironmental conditions. Ironically, the same sea 
level rise that precipitated the formation of es- 
tuarine environments was also a causal factor 
in their disappearance as river-borne sediments 
infilled these coastal features. This explains the 



Paleoenvironment at Almejas 



67 



near absence of estuaries along the modern Pe- 
ruvian coast. 

Clearly, faunal data from the Paijan complex 
sites, the Santa sites, and Almejas are critical to 
address the issue of past climate in the vicinity 
of these sites. In assessing these fauna, partic- 
ularly the fish species, the tendency has been to 
emphasize, and at times "force" the data to 
conform to, the perceived dichotomy between 
(1) species that are characteristic of the warmer 
water off the coast of Ecuador and northern 
Peru and have been classified as warm-tropical 
species and (2) species that are characteristic of 
the cooler water of the Peruvian Current and 
have been classified as warm-temperate species 
(Reitz 1995a, 1995b, 2001; Sandweiss et al. 
1996). To Reitz's credit, she discusses the prob- 
able existence of estuaries in the respective vi- 
cinities of Ostra Base Camp, Almejas, and Pai- 
jan complex sites, states the important charac- 
teristics of estuaries and their fauna, meticu- 
lously reviews habitat data for the species 
identified at the sites, and describes many of the 
fish species identified at the sites as estuarine 
fishes. Nevertheless, in the final analysis, she 
categorizes these typically estuarine fishes as 
warm-tropical species (Reitz 1995a, 1995b, 
2001). In contrast to this approach, we believe 
that the marine fauna of the three sites under 
consideration here should be examined in light 
of the prevalent environments at the sites: es- 
tuaries and offshore warm-temperate waters. 

Tables used by Sandweiss et al. (1996:Table 
3; Reitz 1995a:Table 1, 1995b:Table 2) to show 
broad trends on the basis of MNI (minimum 
number of individuals) percentages for what 
they classified as warm-tropical versus warm- 
temperate fish species resulted in high values 
for warm-tropical species from Paijan sites, Os- 
tra Base Camp in the Santa area, and Almejas. 
Although nonmarine vertebrates figured more 
prominently in the subsistence regimen of the 
Paijan sites, the identifiable fish (MNI =113) 
were assessed at 97.3% warm-tropical species 
versus 2.6% warm-temperate species. For the 
Ostra Base Camp site, the values were 64.2% 
warm-tropical species and 35.8% warm-tem- 
perate species (MNI = 120). For Almejas, the 
values also included mixed-habitat species (spe- 
cies known to occur in both warm-tropical and 
warm-temperate waters), and the column sam- 
ple and general sample were treated separately 
(Reitz 1995a, 1995b). The Almejas results, as 
tabulated by Reitz (1995a, 1995b), were as fol- 



lows: 40% warm-tropical, 35% warm-temper- 
ate, and 15% mixed for the general excavation 
(MNI ---- 114), and 12% warm-tropical, 84% 
warm-temperate, and 4% mixed for the column 
sample (MNI = 131). 

These data presented by Reitz (1995a, 1995b, 
2001) and Sandweiss et al. (1996) would seem 
to indicate the presence of warm offshore wa- 
ters in the vicinities of the three sites. However, 
closer examination of the individual fish species 
and their habitats suggests to the authors that 
most fishes classified as warm-tropical species 
are more appropriately classified as estuarine 
species. This has already been demonstrated for 
Almejas (described above), for which detailed 
data are available to the authors. Once estuarine 
species have been reclassified, few species 
identified at Almejas remain within the warm- 
tropical category (Tables 2 to 4). Detailed spe- 
cies lists for Paijan complex sites have not been 
published; however, Reitz (1995b, 2001) de- 
scribes sea catfish (Ariidae) and lisa (mullet, 
Mugil spp.) as the most common fishes, with 
bonefish (Albula vulpes) and croaker (Micro- 
pogonias spp.) common in some assemblages 
and small numbers of mojarra (Gerridae, Eu- 
cinostomus spp.) and porgy (Sparidae) also 
identified. Herring (Clupeidae), anchovy (En- 
graulidae), and coco (Paralonchurus spp.) were 
also present. Among these species listed for the 
Paijan complex sites, all are commonly found 
in estuaries except adult herring, anchovy, and 
coco (Paralonchurus spp.), which are warm- 
temperate species, and mojarra (Gerridae), the 
only fish listed that is typically taken in warm- 
tropical waters (Reitz 1995b). Fewer data are 
available concerning fish species identified at 
Ostra Base Camp; however, Reitz (1995a, 
2001) mentions bonefish, sea catfish, lisa (mul- 
let), and puffer (Spheroides annulatus) as the 
primary species, with warm-temperate fishes 
relatively rare. All of these primary species 
mentioned for Ostra Base Camp are estuarine 
fishes (Reitz 1995b, 2001). 

Data from the fine-screened column sample 
we excavated at Almejas were also critical to 
our realization that subsistence activities at this 
site were focused primarily on the local estua- 
rine ecosystem and its component resources. 
These tiny bones represent small fishes and es- 
pecially the young of species that typically use 
estuaries as nurseries. Their importance to the 
inhabitants of Almejas is especially evident 
when their respective biomass values are ad- 



68 



S. Pozorski and T. Pozorski 



justed to compensate for the difference in vol- 
ume between the column sample and the gen- 
eral excavation (Table 4). Mud flat mollusks, 
also typical of estuaries, composed the other 
major source of food for the people of Almejas. 
These shellfishes provide additional evidence of 
the importance of this resource zone to their 
subsistence. The location of the site and the in- 
habitants' decision to settle near the mouth of 
the Casma River were likely predicated on the 
rich and abundant estuarine resources, and the 
site was likely abandoned once the estuary silt- 
ed in and disappeared. Nevertheless, the pres- 
ence of substantial amounts of warm-temperate 
fish species along with a number of molluscan 
species known to inhabit warm-temperate wa- 
ters provides evidence that warm-temperate 
species were accessible to and exploited by the 
site's occupants. These species also document 
the presence of the cooler offshore waters of 
the Peruvian Current in the vicinity of the site. 
The data presented and reviewed here reveal 
that the site of Almejas is unusual for several 
reasons. It represents one of the earliest marine- 
oriented sites along the north and central coast 
of Peru, predating by at least 2000 years most 
of the larger, better known sites dating to the 
Late Preceramic Period. Its shellfish and fish 
inventories also distinguish Almejas from most 
known preceramic sites and provide critical ev- 
idence that subsistence activities by the site's 
inhabitants focused on a local estuarine envi- 
ronment complemented by some exploitation of 
warm-temperate offshore waters. Coincident 
geomorphological data indicate that modern sea 
level had been attained by the time Almejas 
was occupied, resulting in the formation of the 
estuarine environment that attracted these early 
settlers. Finally, the faunal remains, the geo- 
morphological data, and archaeological evi- 
dence of optimum preservation argue that the 
ENSO phenomenon has been in existence since 
at least 5000 B.C., and probably much longer. 

Acknowledgments. Permission to excavate at 
Almejas was granted by the Institute Nacional 
de Cultura, and funding for the excavation was 
provided by grants from the O'Neil and Netting 
Funds of the Carnegie Museum of Natural His- 
tory. Funds for the radiocarbon assays were 
provided by grant BNS-8203452 from the Na- 
tional Science Foundation. Vertebrate faunal re- 
mains from Almejas were identified by Eliza- 
beth Reitz of the Museum of Natural History, 



University of Georgia, with funding from the 
Faculty Research Council at the University of 
Texas-Pan American. Interpretations of the re- 
sults of this faunal analysis within this paper, 
including tables constructed by the authors us- 
ing Reitz's identifications and biomass recon- 
structions, reflect the opinion of the authors. 



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The Impact of the El Nino Phenomenon on 

Prehistoric Chimu Irrigation Systems 

of the Peruvian Coast 



Thomas Pozorski and Shelia Pozorski 



Long-abandoned prehistoric irrigation systems 
are a common feature of the landscape in many 
Peruvian coastal valleys. Some of the most im- 
pressive examples of prehistoric irrigation sys- 
tems can be found between the La Leche Valley 
and the Viru Valley on the north coast of Peru 
(Kosok 1965). These remains of canals and oc- 
casional fields, which currently lie outside the 
limits of modern irrigation, are believed to date 
to about B.C./A.D. or later, within Early Inter- 
mediate Period (200 B.C.-A.D. 600) through 
Late Intermediate Period (A.D. 1000-1470) 
times. Studies of these exceptionally well-pre- 
served remains of ancient land reclamation fea- 
tures reveal that their planners and builders 
faced a variety of challenges, including diffi- 
culties presented by local topography, the na- 
ture of the substrate, and periodic climatic var- 
iation, especially the notable impact created by 
strong El Nino rains that hit the Peruvian north 
coast a few times each century. Some challeng- 
es were effectively met through varied and of- 
ten ingenious engineering feats. Other challeng- 
es were never successfully overcome despite 
the expenditure of vast amounts of labor. To 
ameliorate the effects of such engineering fias- 
cos, alternative strategies were developed to 
compensate for production lost as a result of 
failed reclamation efforts. 

The data and conclusions presented here are 
the result of fieldwork within the Moche and 
Chicama Valleys during the late 1970s by the 



Programa Riego Antiguo archaeological pro- 
ject. This project involved intensive survey 
and mapping of the prehistoric irrigation sys- 
tems outside the limits of modern cultivation 
within the Moche Valley, as well as study of 
the area between the Moche and Chicama Val- 
leys traversed by the Chicama Moche Inter- 
valley Canal. All of these areas with preserved 
prehistoric canals were explored further 
through excavations that transected the canal 
channels and by means of occasional horizon- 
tal clearing. The Moche and Chicama prehis- 
toric irrigation systems had been subject to 
surface survey and limited test excavations 
prior to the Programa Riego Antiguo archae- 
ological project (Farrington 1974, 1980; Far- 
rington and Park 1978; Kosok 1965; Kus 
1972). It was evident from the beginning of 
the project, however, that intensive excavation 
would be needed to sort out the complex na- 
ture of these systems and their relationships 
with the prehistoric sites in the area; the so- 
cieties that built, maintained, repaired, and ul- 
timately abandoned them; and the surrounding 
environment that was subjected to periodic El 
Nino rains. Through detailed study of the sur- 
face evidence and excavated canal profiles and 
features, it was possible to develop a detailed 
chronology of the growth and decline of the 
irrigations systems, including when and how 
they were affected by El Nino rain. 



71 



72 



T. Pozorski and S. Pozorski 



Cerro 
Campana / 



Intervalley Canal 



Pampa 



Pampa 
Rio Seco 



, Cerro 
s Cabras 



PampaN 



Esperanza\ Vichansao 
Canal 



Caballo 
Muerto 



Chan 



\> 



N 




Moche River, 



Cerro I 
Blanco 



Modern Cultivation 

Hill 

Bluff 




Figure 1. Map of the Moche Valley showing the extent of modern cultivation, the Three-Pampa area, prehistoric 
canals outside of modern cultivation, and relevant archaeological sites. 



The Archaeological Evidence 

Canals and Fields 

The extremely arid climate of coastal Peru fos- 
ters excellent preservation of archaeological re- 
mains, including the prehistoric agricultural 
features that extend beyond the limits of mod- 
ern cultivation (Figs. 1 and 2). These range 
from major and minor canals to fields with in- 
tact furrows (Fig. 3). Within the Moche Valley, 
several small prehistoric canal systems are pre- 
served on both sides of the river; however, the 
greatest expanse of preserved canals and fields 
lies well down-valley, toward the ocean. This 
latter zone, which contains Pampas Esperanza, 
Rio Seco, and Huanchaco, has been designated 
the Three-Pampa area (Figs. 1 and 2). In late 
prehistoric times, an effort was made to draw 
water into the Three-Pampa portion of the sys- 
tem from the Chicama River in the next valley 
north via the unsuccessful Chicama-Moche In- 
tervalley Canal. This tremendous undertaking is 



well documented in the archaeological remains 
(Kosok 1965:90-94; T. Pozorski 1987; T. Po- 
zorski and S. Pozorski 1982). 

Within the Moche Valley, the largest canals 
in the archaeological record actually represent 
now-abandoned extensions of canals still in use 
along much of their lengths. These canals were 
designed for water transport; they drew water 
directly from the Moche River. A hierarchical 
system of increasingly smaller canals carried 
water from each major canal to associated sets 
of fields. 

Excavations that transected canals and fields 
revealed the history of their construction and 
use or lack of use. As expected, major canals 
contained a succession of numerous channels, 
reflecting their permanence upon the landscape 
and long-term use. Successively smaller canals, 
and especially fields, contain correspondingly 
fewer distinct channels, reflecting the fact that 
smaller elements of the total system were more 
ephemeral. When the profiles of transected ca- 
nals were examined, individual channels could 



Prehistoric Chimu Irrigation Systems 



73 




|/ /\ Modern cultivation 

Figure 2. Map of the Three-Pampa area showing the major irrigation canals that lie north of Chan Chan. 



be distinguished by the nature of their compo- 
nent sediments; and these channels or major 
use episodes could be traced from profile to 
profile along the length of major canals and 
many minor canals. Based on these connections 
among canal channels, it was possible to de- 
velop a sequence for the construction and use 
of the portion of the prehistoric Moche Valley 
canal system outside modern cultivation. 



Evidence of Canal Use 

Profiles of transected canals also yielded infor- 
mation on the duration and intensity of canal 
use. Canal use was reflected archaeological ly 
mainly in two ways. First, within the active 
channel, laminar sediments were formed as wa- 
ter-borne material left in suspension or surface 
deposits blew in and were arranged in a laminar 
configuration by the water flow (Fig. 4). Fre- 
quently, this deposition constituted the process 
by which the initially excavated channel stabi- 



lized in response to water flow. Subsequent 
changes in water velocity or quantity resulted 
in erosion and/or deposition. 

A second indicator of canal use was the dark 
coloration of sediments or soils beneath a chan- 
nel that resulted from water logging. When sed- 
iments are subjected to repeated wet-dry epi- 
sodes, oxidation occurs, turning the surfaces of 
the individual soil particles first yellow to or- 
ange and ultimately brown to dark red. Canals 
observed in profile exhibited varying degrees of 
oxidation from very slight to no discoloration 
to intensive darkening 40 cm or more below the 
active channel. When sediments are kept wet 
for longer periods of time, waterlogging occurs, 
turning soil particles gray to black in color. 

Neither an evaluation of the deposition and 
erosion of water-lain canal sediments nor a con- 
sideration of the amount of associated oxidation 
can be used to reconstruct absolute time spans 
for canal use. However, when taken together, 
they provide a relative indicator of the magni- 
tude of use for a given channel. Based on the 



74 



T. Pozorski and S. Pozorski 




^vT Si?m 

,-.vW '.:. rft-^-Z 



^-^t^* ^T 

6s,:x;. r-'??^ r >g*t.-. 

^^S|^:^ 



<^-r3B^ 




'? - t^^^^Bfcl* : - J^-l r ' "'- ' ;"' ^-. ^-.-x^ 

Figure 3. View of stone-lined Chimii canals along the east edge of Pampa Rio Seco. 



same evidence, canals or channels lacking both 
laminar sediments and oxidation never func- 
tioned effectively. Such abortive canal seg- 
ments often have additional characteristics that 
precluded their effective use, such as an uphill 
slope (T. Pozorski and S. Pozorski 1982). 



Irrigation Systems 
Prior to B.C./A.D. 

Preserved remains of prehistoric irrigation sys- 
tems date relatively late in the Andean se- 
quence; however, there is general agreement 
that irrigation agriculture had its beginning 
much earlier. Most authors (Burger 1992:57; 
Morris and von Hagen 1993:45; Moseley 1992: 
126; Patterson 1985:67; S. Pozorski and T. Po- 
zorski 1987:114; Richardson 1994:64; von Ha- 
gen and Morris 1998:46) date the inception of 
large-scale irrigation agriculture within Peruvi- 
an valleys to the Initial Period (2150-1000 
B.C.). (Dating is based on calibrated radiocarbon 
dates using values supplied in Stuiver and 



Becker [1993].) Experimentation likely oc- 
curred even earlier, during the Late Preceramic 
(3000-2150 B.C.), when most of the population 
was concentrated in large settlements near the 
coast. Small, short canals may have been con- 
structed within or near the active flood plains, 
which are a considerable distance from most 
Late Preceramic sites. Such experimentation 
with water control is suggested by the varied 
inventory of cultivated species at Late Precer- 
amic sites. These include squash, common 
bean, potato, avocado, lima bean, lucuma, gua- 
va, cansaboca, and especially gourd and cot- 
ton industrial plants essential to the lives of 
coastal fishermen (S. Pozorski 1987:16; S. Po- 
zorski and T. Pozorski 1987:113, 1988:95-96; 
T. Pozorski and S. Pozorski 1990:17-18). 

Evidence for Initial Period irrigation is more 
substantial. At this time large, complex sites 
dominated by one or more platform mounds ap- 
pear well inland in over 15 river valleys of the 
north and central Peruvian coast. These mounds 
are located at or near optimum zones for canal 
intakes as if to effectively monitor or control 
water use (Burger 1992:57; Morris and von Ha- 



Prehistoric Chimu Irrigation Systems 



75 




Figure 4. View of laminar deposits within a now-abandoned prehistoric Chimu canal. 



gen 1993:45; Moseley 1992:126; Patterson 
1985:67; S. Pozorski and T. Pozorski 1987:114; 
T. Pozorski 1982; Richardson 1994:64; von Ha- 
gen and Morris 1998:40). In the Moche Valley 
during the Initial Period, the irrigation system 
probably extended down to the Caballo Muerto 
Complex (Fig. 1). Many of the large mounds at 
these sites also face up-valley or upriver, an ori- 
entation that has been correlated with reverence 
for the source of the river water so essential to 
irrigation (S. Pozorski and T. Pozorski 1987: 
114; Williams 1985:230). Subsistence data 
available for this time period document a 
marked increase in the variety and especially 
the quantity of cultivated plants consumed and 
used at Initial Period sites. Peanuts and manioc 
are some of the food plants added to the pre- 
historic diet at this time. Comparisons of sub- 
sistence inventories for coastal and inland sites 
suggest that marine resources continued to be 
important and that satellites of the inland cen- 
ters were established and maintained on the 
coast to supply essential protein in exchange for 
agricultural products (S. Pozorski and T. Pozor- 
ski 1979, 1987:19-20). 



Early Intermediate Period 
Irrigation Systems Within the 
Moche Valley 

Within the Moche Valley, the earliest evidence 
of prehistoric irrigation that expanded beyond 
the limits of modern cultivation dates to the 
Early Intermediate Period and is associated with 
the Moche occupation of the valley. At this 
time, the extent of cultivated land extended 
slightly outside modern limits, encompassing 
only Pampa Esperanza and a narrow strip with- 
in Pampa Rio Seco along the west edge of Pam- 
pa Esperanza (Figs. 5 and 6). With the excep- 
tion of a single canal on Pampa Rio Seco that 
lies near the modern surface, the Moche canals 
are deeply buried, directly underlying subse- 
quent Chimu use of the same channels. 

The Moche and Chimu efforts to reclaim the 
area are distinct, however, and can be distin- 
guished on the basis of several lines of evi- 
dence. Canal channels believed to have been 
constructed during the Early Intermediate Pe- 
riod are often directly associated with Moche 
sites, and their extent corresponds to the extent 



T. Pozorski and S. Pozorski 



N 

2 



4 km 




Blanco 




[/ A Modern Cultivation 
|r-^~| Hill 

K\ v "| Bluff 

Prehistoric Cultivation 

Figure 5. Map of the Moche Valley showing the extent of prehistoric irrigation outside modern cultivation during 
Moche times (A.D. 100-600). 



of substantial Moche occupation of the Three- 
Pampa area. Canal-bank sediments associated 
with these deep channels contained occasional 
Moche ceramics, but no later cultural material, 
and one charcoal sample from a canal bank 
yielded a radiocarbon date of A.D. 550 80 (T. 
Pozorski 1987:Table 1). Finally, the natural 
substrate beneath these canals is the most inten- 
sively oxidized, characterized by dark red col- 
oration, and waterlogged, characterized by near 
black coloration. 



Late Intermediate Period 
Irrigation Systems Within the 
Moche Valley 

Irrigation agriculture within the Moche Valley 
reached its maximum extent during the occu- 



pation of the valley by people known as the 
Chimu (Fig. 7). This state, governed from Chan 
Chan its capital located within the Moche 
Valley dominated the north coast during the 
Late Intermediate Period. The beginnings of 
this state date to about A.D. 900. By about A.D. 
1300, the Chimu state had expanded north and 
south to incorporate lands between the Jeque- 
tepeque and Casma Valleys, thereby dominating 
the area previously governed by the Moche 
state (Donnan 1978:1; Mackey and Klymyshyn 
1990:203-205; T Topic 1990:184-189). This 
was apparently also the time of maximum ag- 
ricultural expansion the time when the Chimu 
implemented an aggressive program of canal 
and field expansion within valleys under their 
control. Motivated by an El Nino flood that ad- 
versely impacted their land reclamation efforts, 
the Chimu altered their strategy and expanded 
their polity much further north and south to en- 



Prehistoric Chimu Irrigation Systems 



77 





Chan Chan 



[/ /j Modern cultivation 

Figure 6. Map of the Three-Pampa area showing the major canals which functioned during Moche times (A.D. 
100-600). 



compass lands as far north as Tumbes and as 
far south as the Chillon Valley (Donnan 1990: 
267; Mackey 1987:121-122; Richardson et al. 
1990:434-436; Rowe 1948; Shimada 1990: 
313). Domination by the Chimu state ended in 
A.D. 1470 as a result of defeat by the expanding 
Inca empire. 

Early Intermediate Period Moche canals un- 
derlie some of the major channels that were 
subsequently used by the Chimu; however, vir- 
tually all of the prehistoric irrigation features 
readily visible on the surface were originally 
constructed by the Chimu. These include small 
systems located well inland on either side of 
the valley as well as the Three-Pampa area 
an unusually large zone of ancient canals and 
fields that extends from the edge of modern 
cultivation toward the ocean (Figs. 1 and 2). 
The Chimu were also responsible for the con- 
ception and execution of the Chicama-Moche 
Intervalley Canal, a massive undertaking to di- 
vert water from the Chicama River 20 km to 
the north and channel it onto the Three-Pampa 
area (Kus 1972; Ortloff et al. 1982; T. Pozorski 



1987:116; T. Pozorski and S. Pozorski 1982). 
The Three-Pampa area, which consists of Pam- 
pa Esperanza, Pampa Rio Seco, and Pampa 
Huanchaco, is an integrated system of canals 
and fields originally fed by two major canals 
on the north side of the Moche River. The 
Three-Pampa area as well as the Intervalley 
Canal that was intended to supplement the wa- 
ter supply for the Three-Pampa area are the 
main focus of this study. 



The Administration of Land Reclamation 

In order to execute tasks as formidable as culti- 
vation of the Three-Pampa area and construction 
of the Chicama-Moche Intervalley Canal, the 
Chimu built rural administrative centers (Keat- 
inge 1974, 1980; Keatinge and Day 1973, 1974; 
T. Pozorski 1987:1 14-1 17). Although these sites 
also likely served to monitor maintenance of the 
irrigation systems as well as production within 
the fields, they were primarily established to 
oversee initial canal and field construction. In 



78 



T. Pozorski and S. Pozorski 



Cerro ' 

Campana / 



Intervalley Canal 



Par 



N 

2 



4 km 




[/ /j Modern Cultivation 
|r-^~| Hill 
|v^ u | Bluff 

Prehistoric Cultivation 

Figure 7. Map of the Moche Valley showing the extent of prehistoric irrigation outside of modern cultivation 
during Chimu times (A.D. 1000-1300). 



this capacity, the rural administrative centers rep- 
resent expansion of the Chimu state onto previ- 
ously unfarmed desert areas, and they are con- 
sistently located in close association with canals 
and field systems (T. Pozorski 1987:114-117). 
Ironically, many of the canals and field systems 
connected with rural administrative centers were 
never fully operational. 

Within the Moche-Chicama Valley area, four 
rural administrative centers have been identified 
and investigated to date. These centers are Que- 
brada Katuay, located well inland on the north 
side of the Moche Valley; El Milagro de San 
Jose, located on Pampa Rio Seco (Fig. 2); Que- 
brada del Oso, located some 3 km south of 
modern cultivation in the Chicama Valley and 
associated with the Chicama-Moche Intervalley 
Canal; and Pampa Mocan, located 3.7 km north 
of modern cultivation in the Chicama Valley 



(Keatinge 1974; Kus 1972:99-102; T. Pozorski 
1987:Fig. 1). 



Challenges, Successes, Failures, and 
Alternative Strategies 

The Chimu faced distinct challenges as they ex- 
panded the Moche Valley irrigation system far 
beyond its previous limits, and especially as 
they endeavored to draw water from the Chi- 
cama River into the Moche system. These chal- 
lenges are directly related to the fact that, once 
the Chimu moved beyond land reclaimed in 
Moche times, they were expanding the irriga- 
tion system into areas not previously cultivated. 
The topography, the nature of the local sub- 
strate, and the lack of adequate water were for- 



Prehistoric Chimu Irrigation Systems 



79 




O 
Phase 1 architecture 



.. Phase 2-3 architecture 



Y A Modern cultivation 



1 Velarde 

2 Squier 

3 Gran Chimu 

4 Bandelier 

5 Laberinto 



Figure 8. Map of the Three-Pampa area showing the maximum extent of canal systems during preflood Chimu 
times (A.D. 1000-1300). 



midable obstacles. Once in place, prehistoric ir- 
rigation systems were also impacted periodical- 
ly by El Nino-related rainfall. 



Topography 

Paramount in the effort to fully reclaim the 
Three-Pampa area was the extension of the Vi- 
chansao Canal, the major canal that drew water 
from the Moche River, so that water could be 
transported to Pampas Rio Seco and Huanchaco 
(Figs. 7 and 8). In doing this, the objective was 
to incorporate the maximum amount of land 
while also creating a functioning canal to pro- 
vide water for this land. The projected route 



was along the north edge of Pampa Esperanza, 
then across Pampa Rio Seco a dry river chan- 
nel, all the while maintaining sufficient eleva- 
tion to provide water to Pampa Huanchaco, an 
area of higher ground on the other side of Pam- 
pa Rio Seco. The Chimu ran the Vichansao as 
high as possible along the valley edge, creating 
a channel with a remarkably shallow slope of 
.0001. As the canal crossed Pampa Rio Seco, 
the channel bottom ran at approximately the 
surface level of the pampa for much of its 
length. This was accomplished by building up 
banks using soil scraped from the nearby sur- 
face to create a channel at ground level, but 
without any elevation of the canal bottom. Fur- 
ther along, to cross lower portions of Pampa 



80 



T. Pozorski and S. Pozorski 



Rio Seco and maintain elevation sufficient to 
supply Pampa Huanchaco with water, a true aq- 
ueduct was constructed, raising both the chan- 
nel and banks above ground level. 

Where the Vichansao was excavated into the 
substrate or ran at ground level, occasional 
abortive channels that take off "uphill" attest 
to the difficulty of the builders' task, and also 
suggest that Chimu engineering efforts were 
characterized by trial and error. Nevertheless, 
the Chimu were able to create a functioning ca- 
nal that traversed varied terrain while maintain- 
ing an extremely low slope in order to maxi- 
mize the amount of land reclaimed. The Vi- 
chansao, and lesser canals within the Three- 
Pampa system, were functioning canals, as 
indicated by laminar sediments and especially 
oxidation. Although the degree of oxidation de- 
creases toward the periphery of the system, 
there is clear evidence of functioning canals all 
the way out to Pampa Huanchaco. This is ample 
testimony to the success of Chimu efforts to 
extend the Moche Valley irrigation system far 
beyond any previous limits. 



Natural Substrate 

In constructing the Vichansao canal, much of 
the canal's channel was cut through a zone of 
aeolian sand banked against Cerro Cabras. 
Sand-filled channels attest to problems with lo- 
cal sand blowing into the canal, and ample sand 
in bank deposits documents successful efforts 
to keep the channel open through regular clean- 
ing. Such porous sand would also have allowed 
much water loss through seepage until suffi- 
cient finer particles silts and sands had ac- 
cumulated to self-line the channel. There was 
little effort to artificially line the channel as a 
means of retarding seepage. Stone lining and, 
rarely, adobe lining on the canal interiors was 
regularly employed where the Vichansao 
crossed Pampas Rio Seco and Huanchaco. 
However, the channel bottom was not lined, and 
sidewall lining apparently functioned more to 
retain loose bank soils than to prevent seepage. 
The same problems of substrate porosity and 
blowing surface sand also impacted smaller 
feeder canals and fields on the Three-Pampa 
area. On Pampa Esperanza, which had been un- 
der cultivation since the Early Intermediate Pe- 
riod, field soils were silt-rich and less porous 
near the surface, allowing for better moisture 



retention. On the other two pampas, especially 
Rio Seco, the substrate was very loose, con- 
sisting of porous, coarse sand to gravel and cob- 
bles. Ironically, although such soils make farm- 
ing the surface difficult at first because so much 
water is lost through evaporation and seepage, 
they also provide near-ideal conditions for 
drainage beneath the fields and canals. This pre- 
vents the buildup of salts that can potentially 
render fields useless. 



Chicama-Moche Intervalley Canal 

The Chicama-Moche Intervalley Canal ranks 
among the most ambitious irrigation projects 
ever attempted on the north coast. It represented 
an effort to bring water from the Chicama River 
across the 70-km-long canal route of rocky, un- 
even desert to the Moche Valley (Fig. 9; T. Po- 
zorski and S. Pozorski 1982:Fig. 1). Although 
a few small areas of fields were laid out or con- 
structed along its course between the two val- 
leys, the Chicama-Moche Intervalley Canal 
was apparently conceived of primarily as a 
means to increase the amount of water available 
for the Three-Pampa area within the Moche 
Valley. Unfortunately, it also proved to be 
among the most noteworthy engineering fiascos 
ever documented archaeologically. 

Evidence of oxidized sediments within the 
main supply canal, the Vichansao, all the way 
to Pampa Huanchaco reveals that the Chimu 
had created a canal that was sufficiently well 
engineered to reach the farthest limits of the 
land they endeavored to bring under cultivation. 
Nevertheless, the magnitude of oxidation within 
the channel decreases markedly along its route 
toward the periphery. This suggests that there 
was rarely sufficient water to keep the farthest 
reaches of the system under cultivation. To rem- 
edy this, about A.D. 1 100 the Chimu embarked 
on a labor-intensive effort to supplement the Vi- 
chansao's flow and provide additional water to 
the entire Three-Pampa area. Evidence of this 
intent comes from the fact that the Chicama- 
Moche Intervalley Canal path circles well 
around the base of Cerro Cabras in order to feed 
into the Vichansao at a point sufficiently up- 
stream to allow access to Pampa Huanchaco 
(Figs. 7 and 9). The system of smaller canals 
(Fig. 9, Canals I and II) taking water from the 
Vichansao to the fields was also redesigned at 



Prehistoric Chimu Irrigation Systems 



81 




Y A Modern cultivation 



Figure 9. Map of the Three-Pampa area showing the reconfiguration of the Moche Valley canal system in 
anticipation of supplemental water from construction of the Chicama-Moche Intervalley Canal. The relationship of 
the Great North Wall and Phase 2-3 architecture of Chan Chan to Canal II is also indicated. 



about the same time in anticipation of the ad- 
ditional water. 

Much effort was expended on the Chicama- 
Moche Intervalley Canal before it was finally 
abandoned. At least one channel which in 
places is quite shallow can be traced across 
its entire intended route. The greatest elabora- 
tion, however, is evident in the portion of the 
canal north of the "divide" the highest point 
topographically which the canal had to traverse 
along its route between the Chicama and Moche 
Valleys. This northern zone is an engineer's 
nightmare because of the uneven terrain, a 
seemingly unending series of quebradas and 



rocky ridges descending from the Andean foot- 
hills. When their first effort to create a func- 
tioning canal failed, the Chimu tried again and 
again, raising the channel each time in the hope 
of attaining sufficient elevation to cross the di- 
vide. This required tremendous effort, especial- 
ly where the canal had to be supported against 
bare bedrock. At several locations the Chimu 
used fire to heat crack the stone, and then cut 
through the bedrock of ridges that impeded the 
canal's progress. Charcoal from these fires pro- 
vided samples for radiocarbon dating (T. Po- 
zorski 1987:113, Table 1). Some segments of 
the canal were rebuilt as many as seven times, 



82 



T. Pozorski and S. Pozorski 



with each successive segment requiring addi- 
tional stone-lined terraces to shore up the down- 
slope bank and support the channel. 

Numerous excavations transecting the Chi- 
cama-Moche Intervalley Canal channel were 
made north of the divide in the vicinity of Que- 
brada de Oso. This location was selected be- 
cause canal construction was especially elabo- 
rate there and a sizable expanse of fields and 
smaller canals was also present. An exception- 
ally large and long aqueduct had also been con- 
structed in this area, across Quebrada del Oso. 
This aqueduct was largely destroyed by El 
Nino-related wash down the quebrada; how- 
ever, this same El Nino destruction exposed a 
cross section of the aqueduct that was cleaned 
as part of the excavations of the Chicama-Mo- 
che Intervalley Canal. 

Despite claims of great Chimu engineering 
skills (Kus 1972, 1984; Moseley 1992:260; Ort- 
loff 1981, 1988, 1993, 1995; Ortloff etal. 1982, 
1985), numerous excavations within the Chi- 
cama-Moche Intervalley Canal yielded no ev- 
idence that the canal had ever effectively car- 
ried water (T. Pozorski 1987:116; T. Pozorski 
and S. Pozorski 1982). Most significantly, there 
was no evidence of oxidation in any of the 
channels. Cuts transecting the canal occasion- 
ally revealed bands of fine sand and silt; how- 
ever, these lacked the laminar structure of mov- 
ing water. These deposits are clearly the result 
of standing water that periodically filled seg- 
ments of the channels during El Nino rains. 
Capture of standing water within segments of 
the channel was facilitated by the undulating 
slope of the canal that resulted from engineer- 
ing error. 

Smaller canals constructed to water the area 
of fields near Quebrada del Oso likewise show 
no evidence of use. Their construction is inter- 
esting, however, because their intakes and chan- 
nels were cut into the bedrock of ridges that 
projected toward the fields. Where these ridges 
ended, soils were mounded up to aqueduct the 
channels into the fields. During the latest effort 
to rebuild the canal, the intakes for these canals 
were filled in, becoming part of the canal bank. 
This ended all efforts to cultivate fields along 
the Chicama-Moche Intervalley Canal route. 

The entire 70-km length of the Chicama-Mo- 
che Intervalley Canal was surveyed on foot as 
well as mapped, and slope measurements were 
made with a 1 -second theodolite. Problems that 
Chimu engineers experienced in their efforts to 



traverse the difficult terrain became readily ap- 
parent during this careful study of the canal. 
They clearly lacked the ability to topographi- 
cally relate the elevation of the intake for the 
Chicama-Moche Intervalley Canal within the 
Chicama Valley to the elevation of the divide 
the highest point the canal would traverse. The 
result was a disastrously blind following of to- 
pography "up and down" as the channel as- 
cended and then descended quebradas. The 
channel was also cut considerably uphill across 
seemingly fiat, but actually ascending, surfaces. 
Among the most notable examples of such en- 
gineering flaws is a 13.8-km segment just south 
of Quebada del Oso where the canal slope goes 
uphill almost 70 m (T. Pozorski and S. Pozorski 
1982:854-860). It would seem that once the 
Chimu engineers left the Chicama Valley prop- 
er, where they had used the cultivated valley 
bottom and the river as their frames of refer- 
ence, they were unable to lay out a functioning 
canal with a downhill slope. 



Impact of the El Nino of ca. A.D. 1300-1350 

In approximately A.D. 1300-1350, an excep- 
tionally strong El Nino event impacted the Pe- 
ruvian north coast. The effect on the Moche 
Valley irrigation system was considerable. Ca- 
nal intakes along the river would likely have 
been washed out, rendering canals inoperable 
until repairs could be made. Damage to canals 
was variable. In situations where El Nino wash 
descended a hillside onto sandy pampa, small 
canals were frequently totally washed away, 
covered over, or filled in as the pampa sedi- 
ments were rearranged by the action of the 
swiftly moving water (Fig. 10). Canals and aq- 
ueducts crossing quebradas were cut, and sub- 
stantial segments were washed away by water 
flowing perpendicular to the canal course. In 
cases where floodwater flow paralleled the ca- 
nal channel, additional water frequently entered 
the channel. Flood water flowing within canals 
that had initially been excavated into sandy sub- 
strate caused considerable damage, often cut- 
ting through the canal bottom and gouging out 
a much deeper channel (Fig. 11). Floodgate 
flowing within canals initially excavated into 
rocky substrate caused less damage. Finer silt 
and sand particles were washed from around 
larger stones that came in contact with the 



Prehistoric Chimu Irrigation Systems 



83 



Postflood channel 




20 40 cm 



Figure 10. Profile of a small north-south feeder canal parallel to and east of Canal II in a sandy area on Pampa 
Esperanza. On the left are the remnants of the original channel, partially collapsed and then buried by El Nino wash 
that hit the canal laterally. On the right is a reconstructed post-flood channel built over the flood sediments. This 
second channel was never a functioning canal. 



floodgate, and the surfaces of the stones were 
scoured to a blue-gray color. 

Such extensive damage made irrigation of 
the Three-Pampa area impossible until repairs 
could be made. Some efforts to reactivate the 
system are readily evident in the archaeological 
record. Where canals had been totally washed 
away or obscured, new channels were built 
(Fig. 10). Gouged-out segments were infilled to 
approximately restore original slope (Fig. 11). 
Segments of canals cut by perpendicularly 
flowing water were also rebuilt. At times this 
involved rerouting the channel above and 
around the break to maintain the downhill slope 
within a flood-enlarged gully or quebrada. 

Instances where transverse cuts were repaired 
were particularly instructive regarding the mag- 
nitude of the El Nino event of ca. A.D. 1300- 
1350. Characterization of this event as unusu- 
ally severe reflects evidence from canal recon- 
struction suggesting that no subsequent El Nino 
had comparable impact. Survey data from the 



Three-Pampa area reveal that sizable segments 
of some canals were washed out. Some new 
channels were built by the Chimu to reconstruct 
canals at these locations. These new channels 
are distinct from the earlier canal construction, 
and have not been affected by later El Nino 
activity. Other new channels have been tran- 
sected by subsequent washes. None of the sub- 
sequent damage, however, comes close in mag- 
nitude to the swath cut by the A.D. 1300-1350 
El Nino wash (see below, however, for a cau- 
tionary note on this interpretation). 

Within the Three-Pampa area, efforts to re- 
pair the irrigation system were extensive; how- 
ever, excavation within these channels revealed 
that the reconstructed system was never effec- 
tively used. Laminar sediments within channels 
are minimal, and there is no evidence of the 
associated oxidation indicative of significant 
wetting and drying. Most channels pertaining to 
this latest reconstruction are also considerably 
smaller than preceding uses of the canal. These 



Original channe 



Original channel 




Figure 11. Profile of Canal II near its north end. The original channel was a functional canal showing signs of 
laminar deposits and oxidation. Then the center of this channel was gouged out by swiftly flowing El Nino wash off 
Cerro Cabras that flowed down the route of Canal II. Water flowed around a large boulder, and then, as the flow 
subsided, sediment was deposited. Finally, a reconstructed post-flood channel, which was never functional, was built 
above the flood-deepened channel and its deposits. 



84 



T. Pozorski and S. Pozorski 



less substantial, unused canals represent the fi- 
nal, unsuccessful effort to irrigate the Three- 
Pampa area. Clearly, reclamation of the Three- 
Pampa area was no longer a priority for the 
Chimu. 

Despite efforts to reconstruct the system, the 
Three-Pampa area was never effectively 
brought back under cultivation after the A.D. 
1300-1350 El Nino. The timing of this disaster 
also coincides with the latest dates for the Chi- 
cama-Moche Intervalley Canal, indicating that 
its construction was halted at the same time. 
The devastating effects of El Nino appear to 
have been a catalyst that motivated the Chimu 
to abandon both their unsuccessful efforts to 
bring Chicama water to Moche canals and fields 
as well as their previously successful efforts to 
reclaim the relatively marginal Three-Pampa 
area which the Chicama-Moche Intervalley Ca- 
nal was supposed to have helped irrigate. Pos- 
sibly to compensate for production lost due to 
abandonment of the Three-Pampa area and for 
labor wasted on the Intervalley Canal, the Chi- 
mu changed their strategy and began to look 
outside the Moche Valley for support. 



Alternative Strategies 

The sequence for canal construction and use on 
the Three-Pampa area can be correlated with 
the construction sequence for the compounds at 
the Chimu capital of Chan Chan, immediately 
south of Pampa Esperanza (Figs. 1 and 9). Gen- 
erally, investigators agree that these compounds 
served as palaces for the rulers of the Chimu 
empire (Day 1980, 1982; Klymyshyn 1982; Ko- 
lata 1982). Although there is disagreement 
about the exact order of construction of the 
compounds (Klymyshyn 1987:101-102; Kolata 
1990; Topic and Moseley 1983:158-162), a 
general three-phase construction has been de- 
veloped by Kolata (1982) based on the shape 
of adobe bricks used to build the major com- 
pound walls. Of the ten monumental com- 
pounds, four (Chayhuac, Uhle, Tello, and La- 
berinto) make up Phase 1. Phase 2 consists of 
the Gran Chimu compound and various asso- 
ciated walls to the north of that compound, in- 
cluding the Great North Wall that bounds the 
south side of Pampa Esperanza (Fig. 9). Phase 
3 consists of the five remaining compounds 
(Squier, Velarde, Bandelier, Tschudi, and Riv- 
ero). Since the publication of Kolata's original 



sequence, many other investigators, including 
Kolata himself, have proposed more detailed 
construction sequences based on analyses of ar- 
chitectural elements within the compounds such 
as audencia shape, burial platform configura- 
tion, and entry courts, as well as associated ce- 
ramics (Klymyshyn 1987:101-102; Kolata 
1990; Topic and Moseley 1983:158-162). All 
of these sequences, however, represent only mi- 
nor variations on Kolata's original 1982 se- 
quence and have little bearing on the overall 
relationship between the monumental com- 
pounds and the Three-Pampa irrigation area. 
Therefore, for the purposes of this discussion, 
we will follow the original Kolata sequence. 

During the construction of the Phase 1 Chan 
Chan compounds, when the site was in its ear- 
lier stages of growth, the irrigation system 
reached its maximum extent. Effecting their ag- 
ricultural expansionist policies through rural ad- 
ministrative centers, the Chimu attempted to re- 
claim inland areas on both sides of the valley, 
incorporated the entire Three-Pampa area, un- 
dertook construction of the Chicama-Moche In- 
tervalley Canal, and expanded Chicama Valley 
irrigation systems beyond modern limits. Ar- 
chaeological data indicate that use of the ex- 
panded Moche Valley irrigation system was 
abruptly interrupted between A.D. 1300 and 
1350 by a devastating El Nino event. Despite 
efforts to reconstruct the system, reclamation of 
the more marginal zones of the Moche Valley 
agricultural system was effectively curtailed at 
about this time, and work on the Chicama-Mo- 
che Intervalley canal also ceased. The same El 
Nino event likely caused similar damage in oth- 
er north and north-central coast valleys. 

Chan Chan, however, continued to develop 
after the flood. Five compounds (Phases 2 and 
3), comprising about half the area of Chan 
Chan, were built after the irrigation system had 
shrunk to approximately its modern limits. The 
key to this dating is the relationship between 
Canal II on Pampa Esperanza and the Great 
North Wall which is part of the Phase 2 con- 
struction at Chan Chan (Figs. 9 and 12). Canal 
II, which was part of the reworking of the 
Three-Pampa irrigation system in anticipation 
of water from the Intervalley Canal, is one of 
the latest canals to be built on Pampa Esperanza 
(Fig. 9). This canal contains sediment and oxi- 
dation associated with its original use plus de- 
posits associated with the A.D. 1300-1350 flood 
within its channel (Fig. 12). The Great North 



Prehistoric Chimu Irrigation Systems 



85 




20 40 cm 



Figure 12. Profile of Canal II near its south end. The original channel was a functional canal complete with 
laminar deposits and oxidation. Subsequently the El Nino wash entered the channel, scouring out a small depression 
and leaving flood-borne deposits. Finally, a major east-west segment of the Great North Wall of Chan Chan, here 
composed primarily of adobe, was constructed over both the original channel and the flood sediments within this 
portion of the Canal II. 



Wall, which is part of the Phase II construction 
of Chan Chan, was clearly built over Canal II. 
Thus, at least one-half of the visible compounds 
at Chan Chan postdate the time when the 
Three-Pampa area was most effectively irrigat- 
ed. The minor, and largely unsuccessful, efforts 
at canal reconstruction on the Three-Pampa 
area after the A.D. 1300-1350 flood could par- 
tially overlap with the building and use of the 
Phase 2 architecture of Chan Chan, but are un- 
likely to date any later. 

The devastating El Nino flood that curtailed 
reclamation efforts was likely a key factor in 
changing Chimu strategy. Rather than expend- 
ing excessive labor to maintain fields in mar- 
ginal lands, the Chimu apparently formed ad- 
ditional military units and set out to expand 
their domain into more northern and southern 
lands from which tribute could be extracted. 
Strategically, this was an optimum time to take 
advantage of rival polities that had been weak- 
ened by the El Nino disaster, especially farther 
north, where the impact was likely more severe. 



This second, more far-reaching phase of Chimu 
expansion was likely motivated not so much by 
the desire for agricultural products as by the 
desire to gain access to and control over the 
production of artisan goods, especially the met- 
alworking that had been so successfully con- 
trolled from the Lambayeque area (Shimada 
1982:178-179; T. Topic 1990). Within the ca. 
1 50-year span between the flood of A.D. 1 300- 
1350 and their defeat by the Inca, the Chimu 
quadrupled the area they controlled. 

This example from the Moche Valley and 
surrounding north coast areas dominated by the 
Chimu reveals some surprises regarding state 
development in the Andean area. Clearly, irri- 
gation agriculture provided the subsistence base 
that allowed a certain level of political devel- 
opment by the Chimii. It is not the case, how- 
ever, that the maximum extent of land recla- 
mation for agriculture coincided with the max- 
imum extent of state development and Chimii 
polity expansion. During the time between ca. 
A.D. 1050 and the flood of A.D. 1300-1350, 



86 



T. Pozorski and S. Pozorski 



when the Chimu invested so much labor in ca- 
nal and field-system construction, their political 
control extended over relatively few valleys. 
Subsequently, as a result of a distinct strategy 
that focused on more effective control and use 
of human labor and craft production, the Chimu 
emerged as an empire spanning 1,300 km of 
coastal Peru and rivaling the Incas. 



Detecting El Nino Evidence in the 
Archaeological Record: 
A Cautionary Note 

It is clear that evidence of past El Nino events 
can be detected in the archaeological record of 
the desert coast of Peru (Moseley 1992:215, 
254; T. Pozorski 1987:113; Shimada 1982:180). 
The stronger the El Nino event, the more likely 
it is to have a direct impact on archaeological 
remains. Such impacts can be detected as 
washed-out areas or distinct laminar deposits in 
irrigation features, as shown in this paper, or in 
association with architectural features (Uceda 
and Canziani 1993). 

Detecting individual El Nino events at single 
archaeological sites is one thing; however, con- 
necting those events with apparently similar- 
looking events at other sites and areas, either 
within the same valley or in other valleys, is a 
much more difficult task. The ability to inter- 
connect El Nino events over increasingly large 
areas along the coast of Peru would be a pow- 
erful chronological tool that could provide dat- 
ing precision unmatched by any other dating 
means available in Peru. Furthermore, the im- 
pact of strong El Nino events could also pro- 
vide potential explanations for cultural changes 
in the archaeological past (von Hagen and Mor- 
ris 1998:22). 

There are two main problems with El Nino 
correlation in the archaeological record. The 
first problem is chronology. Precise dating is 
essential for correlating El Nino events, wheth- 
er one is connecting areas or sites within a val- 
ley or across many valleys. In the present dis- 
cussion, it is postulated that a major El Nino 
hit the Moche Valley irrigation system around 
A.D. 1300-1350, resulting in major repercus- 
sions on Chimu political strategy. However, 
some authors have dated this flood two centu- 
ries earlier, to A.D. 1100 (Moseley 1992:254; 
Nials et al. 1979). Furthermore, this Moche Val- 



ley flood has been correlated with an A.D. 1 100 
flood that occurred in the Lambayeque region 
(Moseley 1992:252-254; Richardson 1994: 
143). We believe that the stratigraphic evidence 
correlating the flood with the construction se- 
quence of Chan Chan supports an A.D. 1300- 
1350 date for the Moche Valley El Nino and 
that it represents an event distinct from the 
Lambayeque A.D. 1100 El Nino. It is apparent, 
however, that there is substantial disagreement 
on this correlation. 

This single example points out the chrono- 
logical problem with El Nino correlation. Here 
are two El Nino events, separated in time by 
two centuries, that are nevertheless the source 
of chronological controversy. The problem can 
only get more complicated as one deals with El 
Nino events more closely spaced or more dis- 
tant in time. Given that major El Nino events 
affect much of the north and central Peruvian 
coast at least two or more times per century, 
and given the relative grossness of dating meth- 
ods currently available, archaeologists will be 
hard-pressed to distinguish and date El Ninos 
that occur within 50 years of one another, let 
alone within 15 years, as is the case with the 
recent 1983 and 1998 floods. 

A second, potentially even more difficult 
problem is the spatial correlation of strong El 
Nino events. We were able to correlate the im- 
pact of a strong El Nino event over a fairly 
large area of land by carefully studying strati- 
graphic relationships of linear features (canals, 
walls, roads) that intersect in certain places. 
Most archaeological contexts are not character- 
ized by such linear features, instead involving 
sites or features that are separated spatially by 
many kilometers. In some instances, a fairly 
strong case can be made for correlating a single 
El Nino between two sites. For example, in the 
Casma Valley, a major El Nino hit the site of 
Cerro Sechin around 1200 B.C. Here, a recon- 
structed floor built on top of a filled-in corridor 
behind the main mound trapped a pool of water 
that softened the clay floor, which was then trod 
upon by several individuals (Fuchs 1997:150- 
152). Some 5 km away, at the site of Pampa de 
las Llamas-Moxeke, what were likely the same 
El Nino waters fell, damaging portions of friez- 
es on the main mound (Huaca A) as well as 
wetting the floor of an adjacent enclosure upon 
which several individuals trod, similar to the 
Cerro Sechin case (Fig. 13). 

The Casma Valley case just described is en- 



Prehistoric Chimu Irrigation Systems 



87 




Figure 13. Human footprints on the floor of an enclosure adjacent to Huaca A at the Initial Period site of Pampa 
de las Llamas-Moxeke in the Casma Valley. The enclosure floor was wetted heavily by an El Nino event dated to 
about 1200 B.C. 



tirely plausible, given the available stratigraphic 
and radiocarbon evidence, but is by no means 
conclusively proven. It is often assumed that 
major El Nino events will bring rains that will 
more or less uniformly blanket the entire area 
adjacent to the ocean zone that is penetrated by 
the Ecuadorian Countercurrent. Observations of 
rainfall patterns of the 1983 and the 1998 El 
Ninos indicate otherwise. Along the north and 
north-central coast, some valleys were hit hard- 
er than others. Most rainfall came down well 
inland from the coastline, between elevations of 
1000 and 1500 m. Geologically, riverbeds were 
quite changed as river channels were deepened, 
substantially widened, and scoured of vegeta- 
tion. This was quite evident during the 1998 
event for every valley between Chicama and 
Huarmey. 

Archaeological sites and modern settlements, 
however, were more variably affected. In the 
Casma Valley, the Late Intermediate Period 
adobe mound site of Sechin Bajo was complete- 
ly washed away by the swollen Sechin River. 
One kilometer away, the Initial Period site of 



Sechin Alto, situated a few hundred meters 
south of the Sechin River, was only minimally 
affected by rainfall that resulted in a few thin 
patches of silt that settled from small puddles 
of water. In the modern town of Casma, there 
were episodes of rainfall during March 1998. 
During one particularly heavy downpour that 
lasted some two hours, the south part of town 
was drenched by several centimeters of rain, 
whereas the north part of town, 0.5 km away, 
received less than 1 cm of rain. This uneven 
distribution of rainfall during El Nino events 
should not be surprising to anyone who has ex- 
perienced rainfall, and there is no reason to as- 
sume that El Nino rainfall patterns should be 
any different. 

The main point of this discussion is to high- 
light the difficulties of El Nino correlation. 
There are problems associated with both the 
temporal and spatial correlations of El Nino 
events documented from different areas of 
coastal Peru. El Nino events that leave abun- 
dant evidence in several places can potentially 
reveal important chronological and cultural in- 



88 



T. Pozorski and S. Pozorski 



formation, yet careful study is needed to make 
precise correlations. A more difficult task is the 
correlation of El Ninos that leave behind only 
widely scattered pieces of evidence. What ap- 
pears to be a major El Nino event in one valley 
may leave only minimal or no evidence in an- 
other valley or even in another part of the same 
valley. The absence of evidence of an El Nino 
event at a particular site does not mean that 
such an event did not happen. All this means is 
that the particular El Nino event did not happen 
to affect the one site in question. What remains 
a challenge to both archaeologists and geomor- 
phologists alike is the documentation and cor- 
relation of El Nino events and their physical 
and cultural effects. This can only be done 
through a long series of careful, detailed studies 
that will need to be carried out over the next 
few decades. 

Acknowledgments. Funding for the Programa 
Riego Antiguo investigation of prehistoric irri- 
gation systems was provided by National Sci- 
ence Foundation grants BNS76-24538 and 
BNS77-24901. Permission to excavate was 
granted by the Peruvian Institute Nacional de 
Cultura. The authors thank Michael E. Moseley 
for the opportunity to serve as codirectors of 
the project; to Eric E. Deeds for his hard work 
as part of the project, particularly in survey, 
mapping, and the recognition of archaeological 
evidence of El Nino; and to geologist Fred 
Nials for his help in interpreting both cultural 
and natural soils associated with irrigation fea- 
tures. 



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El Nino, Early Peruvian Civilization, and Human Agency: 
Some Thoughts from the Lurin Valley 



Richard L. Burger 



The role of El Nino in the rise and fall of early 
Andean civilizations has attracted increasing at- 
tention over the past two decades as more has 
become known about the role of climate change 
in human history. It is no coincidence that this 
greater sensitivity to climate change in the ar- 
chaeological past has emerged as we have be- 
come increasingly anxious about global warm- 
ing and the way it could affect our future. As 
science has focused more intently on global cli- 
matic change, new methods and theories have 
been developed that allow us to reconstruct past 
climates and to appreciate the degree of vari- 
ability that has existed in the Holocene climate, 
of which the El Nino phenomenon is but one 
small piece. 

The past two decades also saw two major El 
Nino events. As a consequence, many archae- 
ologists working in Peru have experienced, ei- 
ther firsthand or through media coverage, the 
devastation that a major El Nino event can pro- 
duce. By contrast, in 1980, only the most senior 
archaeologists had personally experienced a 
major Nino event, and most academics had to 
rely on accounts of the 1925 El Nino to imagine 
what its effects were like. Thus, historical hap- 
penstance has placed scholars in a situation 
where there are now both personal experience 
and the academic predisposition to take El Nino 
seriously in the archaeological modeling of civ- 
ilizational trajectories in the distant past. Such 
was not always the case. In the late 1960s, for 
example, both Edward Lanning (1967) and Luis 
Lumbreras (1969) found it possible to write 



syntheses of Andean prehistory with barely a 
reference to the El Nino phenomenon, and the 
immediately previous generation of scholars, 
such as Bushnell (1957) and Bennett and Bird 
(1960), ignored El Nino entirely. Such an ap- 
proach has now been largely supplanted, as ev- 
idenced by the work of Michael E. Moseley 
(1992) and James Richardson III (1994), in 
which El Nino figures prominently as a possible 
contributing factor to the emergence, expansion, 
reorganization, and demise of multiple Peruvian 
cultures, including those of Chavfn, Moche, and 
Chimu. 

Recent archaeological literature on the pos- 
sible effect of El Nino on Andean prehistory 
has usually focused on the role of El Nino in 
the evolution of Andean civilization. A classic 
example was a 1981 article by David Wilson, 
in which he posited the El Nino phenomenon 
as a limiting factor in the development of an 
early maritime civilization in the Central Andes 
because of the unpredictable but radical reduc- 
tion in maritime carrying capacity along the 
coast during major El Nino events. In a more 
recent 1999 synthesis, Wilson (1999:352-356) 
updated his earlier argument and suggested that 
the stresses caused by El Nino could help ex- 
plain how a primarily maritime-oriented people 
might accept agriculture as an alternative strat- 
egy, thus creating the conditions for the emer- 
gence of complex society. In the models pro- 
posed by Wilson and others, El Nino is seen as 
shaping a long-term evolutionary trajectory as 
cultures become adapted to their environmental 



90 



El Nino, Early Peruvian Civilization, and Human Agency 



91 



conditions; the role of human actors and their 
strategies is seen as secondary to larger evolu- 
tionary processes. Not surprisingly, such mod- 
els have been criticized as treating humans as 
fundamentally passive and as constructing so- 
cial change merely as a process of reacting to 
natural phenomena, such as natural disasters or 
long-term changes in climate. Although such 
models have merit, it also is important to con- 
sider whether the peoples of pre-Hispanic Peru 
anticipated the dangers posed by El Nino events 
and whether they were able to develop strate- 
gies to mitigate them. In adopting this second 
approach, we recognize that human agency 
played an important role in determining cultural 
stability and change in the past, just as it does 
in the present. 

In the modern world, major disasters are 
most successfully dealt with at the level of the 
nation-state or international community. For ex- 
ample, 90% of the $14 billion in aid to the vic- 
tims of the 1994 California earthquake came 
from the federal government of the United 
States rather than from local or state sources, 
and in Honduras, virtually all aid to alleviate 
the devastation wreaked by Hurricane Mitch 
has come from governmental and charitable 
sources outside of Central America (Davis 
1998). But what disaster strategies were em- 
ployed prior to the emergence of such over- 
arching social and political structures? 



Possible Pre-Hispanic Responses to 
El Nino Events in the Central 
Andes 

In the absence of state-based systems, one way 
of dealing with recurring environmental disrup- 
tions such as El Nino is for families or small 
social units to develop links with distant com- 
munities that are less likely to be affected by 
the environmental perturbation. In the case of 
the northern and central coast of Peru, for ex- 
ample, longstanding links with adjacent high- 
land communities would have facilitated a pre- 
historic alternative to current disaster relief, 
perhaps under the rubric of fictive kinship ob- 
ligations or gift exchange. At the 1982 confer- 
ence on Early Monumental Architecture at 
Dumbarton Oaks, I suggested that in combina- 
tion with the dietary needs of highlanders (e.g., 
for iodine and salt), the danger presented by El 



Nino events would have favored the establish- 
ment of ties between highland and coastal 
groups that could be mobilized in times of di- 
saster. Llama caravans could have brought 
highland agricultural produce down to com- 
munities where an El Nino had devastated both 
the year's crops and maritime productivity 
(Burger 1985:276). 

A modern version of such a strategy was 
mentioned in Robert Murphy's description of 
the 1925 El Nino, in which food shortages on 
the central coast were solved by "mutton on the 
hoof" driven down from the high grasslands 
(puna) and by pack trains of llamas, horses, and 
burros from the highland valleys carrying po- 
tatoes and other foodstuffs (Murphy 1926:46). 
The continued viability of agricultural systems 
in the northern highlands during the last two 
major Nino events supports the plausibility of 
this idea. 

Moreover, recent research by Ruth Shady 
(1997) at Caral in the Supe Valley and by She- 
lia and Thomas Pozorski (1992) at Huaynuna 
and Pampa de las Llamas in Casma has rein- 
forced our appreciation of the Late Preceramic 
and Initial Period links between the highland 
societies involved in the Kotosh Religious Tra- 
dition and their contemporaries in centers on 
the coast. Unfortunately, the hypothesis of high- 
land economic assistance to coastal settlement 
during El Nino events has yet to be tested on a 
microlevel by studying examples of a Late Pre- 
ceramic or Initial Period center that coped with 
an El Nino event. It would be fascinating to 
know if the survival strategy of such a site was 
characterized by refuse that included a sharp 
increase in the amounts of highland meat and 
agricultural produce to compensate for the dis- 
ruption of marine and lower-valley agricultural 
resources. 

In Andean archaeology, one of the rare in- 
stances of a local-level analysis of a prehistoric 
community struggling to deal with an El Nino 
event is the study of two Chimu settlements in 
the Casma Valley by Jerry Moore (1991). 
Moore not only used archaeology to document 
the occurrence of a fourteenth century A.D. El 
Nino event, he also explored some of the cul- 
tural responses to it. He concluded that imme- 
diately following a powerful El Nino, the Chi- 
mu state established a complex of ridged fields 
in order to reclaim waterlogged soils, and an 
adjacent community to house agricultural work- 
ers. This subsistence system was apparently 



92 



R. L. Burger 



maintained for no more than a few years, while 
the normal farming system was restored, after 
which time the site was abandoned. According 
to Moore, by shifting to the cultivation of fields 
that were not irrigated, along with exploiting El 
Nino-resistant species of shellfish, it was pos- 
sible to support the continued occupation of the 
Casma Valley and its administrative center at 
Manchan despite the devastation wreaked by a 
major El Nino event. This case is particularly 
interesting because it illustrates how one pre- 
Hispanic group consciously combined two of 
many possible strategies in order to cope with 
the conditions created by El Nino. In this case, 
the rains from El Nino may have created the 
opportunity for successful dry-farming in this 
section of the normally arid coast. 

Given recent history, it should not be news 
to anyone that El Ninos produce occasional op- 
portunities as well as serious problems. One has 
only to recall the scandal that occurred during 
the 1982-1983 El Nino, when several high- 
ranking military men were accused of using 
army cargo planes to fly cattle down from Pan- 
ama to graze on the vast pasturelands that had 
appeared in Peru's Sechura Desert. The appear- 
ance of more robust lomas vegetation, the mi- 
gration of new kinds of fish, the short-term 
availability of new land for rainfall farming, 
and the sprouting of new pastures may be only 
small consolation when weighed against the 
enormous losses occasioned by an El Nino 
event, but such factors may have been crucial 
for crafting locally based survival strategies in 
pre-Hispanic times. Additional studies along the 
lines of the Casma research should yield greater 
insight into the significance of these alterna- 
tives. It should be noted that the strategy pos- 
ited by Moore for Casma involved the inter- 
vention of state institutions, which were absent 
in much earlier prehistoric times. 



Pre-Hispanic Human Agency, 

El Nino, and the Manchay Culture 

Thus far I have explored some of the possible 
short-term responses to the effects of El Nino 
events in the pre-Hispanic Central Andes. How- 
ever, as geographer Kenneth Hewitt has ob- 
served, "Most natural disasters are character- 
istic rather than accidental features of the places 
and societies where they occur" (Davis 1998: 



52). In the longer-term perspective, humans can 
be considered agents that, with the accumulated 
knowledge of their landscape, either learn to 
anticipate potential disasters and avoid them or 
choose to ignore the dangers and place them- 
selves in harm's way. Mike Davis's book, The 
Ecology of Fear (1998), provides an excellent 
illustration of this perspective. He shows how 
flawed human decisions acted to turn tectonic 
and climatic forces into major dangers in the 
course of human settlement in southern Cali- 
fornia. 

Following in this line of thought, I want to 
consider here whether the coastal societies of 
Peru during the second millennium B.C. (known 
as the Initial Period) perceived the possible 
threat posed by the El Nino phenomenon, and 
if they did, what actions they may have taken 
to protect themselves. In the Central Andes, this 
period of time is of particular interest to those 
interested in the relationship between El Nino 
and the appearance of complex societies be- 
cause it was the time of the emergence of the 
region's earliest civilizations. Among the ac- 
complishments of the coastal cultures of the Ini- 
tial Period were the creation of abundant mon- 
umental architecture, the production of sophis- 
ticated public art, breakthroughs in metallurgi- 
cal techniques, and the building of extensive 
irrigation systems. This Initial Period culture, 
characterized by massive civic-ceremonial cen- 
ters with a U-shaped layout, extended along the 
central coast from Chancay Valley on the north 
to Lurin Valley on the south. Investigations of 
these U-shaped centers of Manchay culture by 
myself and Lucy Salazar (Burger 1992:60-75; 
cf. Silva and Garcia 1997) have focused on the 
southernmost of these valleys, which is located 
immediately south of contemporary Lima, and 
the following commentary is based on our on- 
going research. 

During the second millennium B.C., the pop- 
ulation in the lower Lurin Valley gradually in- 
creased, as reflected in the founding of civic- 
ceremonial centers that served as the focus of 
small-scale social units. Only one such center 
is known to have existed in 1800 B.C., but by 
1000 B.C., at least six such centers appear to 
have been functioning in the lower valley, and 
several more in the middle valley (Fig. 1). 
These centers appear to have been autonomous 
and were not organized by an overarching state 
apparatus; the latter appeared only much later 
in the prehistory of the central coast. The pop- 



El Nino, Early Peruvian Civilization, and Human Agency 



93 




CENTROS DBL PBRIODO INIC1AI 

VALLK OB LUMIM 



Figure 1. The location of Initial Period U-shaped pyramid complexes in the lower Lurin Valley, Peru. (Map 
drawn by Bernadino Ojeda.) 



94 



R. L. Burger 



ulation supporting these centers survived on a 
mixed subsistence system based on irrigation 
farming of crops such as squash, peanuts, 
beans, red pepper, guava, pacae, and lucuma, as 
well as yet unidentified tubers (sweet potato?), 
manioc, and a small amount of maize. These 
domesticated crops were supplemented by the 
collection of wild plants, the acquisition of fish 
and mollusks from the Pacific shore, and the 
hunting of deer, camelids, vizcachas, and birds 
from nearby lomas and riverine environments 
(Benfer and Meadors 2002; Burger and Salazar- 
Burger 1991; Umlauf 2002). 

The largest of the valley's centers, Mina Per- 
dida, was occupied for about a thousand years 
(calibrated C14 years) without evidence of hi- 
atus or abandonment (Burger and Salazar-Bur- 
ger 1998, 2002). If one accepts the proposition 
that the pattern of El Nino events was estab- 
lished by 5,800 years ago (Rollins et al. 1986), 
the Manchay culture in Lurin presents an ex- 
ample of cultural continuity and resilience for 
at least ten centuries in the face of the major El 
Nino events that must have occurred during this 
time. Even if one accepts that El Nino had a 
longer recurrence interval until 3200-2800 cal 
B.P. (Sandweiss et al. 2001), the centers of the 
Manchay culture would still have experienced 
numerous major El Nino events, a fact con- 
firmed by the research I shall describe below. 

Considering the dangers posed by El Nino 
events, the choice of location for Lurin's 
U-shaped centers was not auspicious; in fact, to 
use Mike Davis's phrase, it could be said that 
the groups living in the lower Lurin Valley 
chose to place their centers in harm's way. The 
public complexes were generally built at the 
mouth of deeply cut ravines (quebradas). These 
quebradas were normally bone dry, but they 
sometimes carry water during El Nifios. Such 
locations may have been chosen because they 
provided expanses of relatively level land ad- 
jacent to the valuable irrigated bottomlands of 
the valley. Moreover, the nearby rocky ravines 
and barren valley sides offered ample building 
materials, including stone blocks and lenses of 
clay suitable for mortar and adobes. Unfortu- 
nately for the inhabitants of these centers, the 
loose rock, rubble, and earth in these quebra- 
das, which make such good building materials 
under normal circumstances, are incorporated 
into landslides and debris flows when heavy 
rainfalls occur in the lower Lurin Valley during 
major El Nino events. 



Manchay Bajo and Its Monumental Wall 

Judging from the results of fieldwork in 1998 
and 1999 by the Yale University Lurin Valley 
Archaeological Project at Manchay Bajo, the 
Initial Period occupants of Lurin not only were 
aware of the danger posed by an El Nino event, 
they consciously worked to protect themselves 
against potential disasters. Manchay Bajo 
(PV48-147) is located in the lower valley, 12 
km inland from the Pacific, at 140 m above sea 
level (masl). In contrast to the U-shaped com- 
plexes of Mina Perdida and Cardal, Manchay 
Bajo is on the northern bank of the Lurin River, 
only 800 m from the current course of the river. 

Manchay Bajo is, in most respects, a typical 
U-shaped complex. The archaeological com- 
plex is dominated by a terraced, flat-topped 
central pyramid (Fig. 2), and the site is oriented 
to the northeast. The pyramid, found at the apex 
of the U, measures 100 X 75 m at its base and 
rises 13m above the current level of the valley 
floor. Two elongated lateral mounds, one of 
which is attached to the main pyramid, flank a 
central plaza that is 3 hectares in area (Fig. 3). 
Although lower than the main mound, the lat- 
eral mounds are of considerable size, with 
heights of 1 1 m and 8 m, respectively. The area 
of the site, roughly 20 hectares, and the scale 
of the monumental architecture are slightly 
larger than at Cardal, which is located 1.7 km 
away on the other side of the river. The exca- 
vations at Manchay Bajo revealed a long his- 
tory of construction at the center that included 
a minimum of nine superimposed central stair- 
ways, three superimposed atria, each with mul- 
tiple renovations, and at least nine major build- 
ing episodes. Thus, the large public construc- 
tions seen today were the result of repeated 
constructions that spanned at least six centuries. 

Most of the ceramics associated with the 
monumental constructions date to the late Initial 
Period (approximately 1200-800 cal. B.C.). This 
is consistent with an AMS measurement of 
3010 60 (AA 3442), which, when calibrated, 
has a 2a range of 1404-1052 B.C.; the specimen 
tested comes from a fiber bag (shicra) used to 
hold stone in the fill covering the site's middle 
atrium. Since this measurement dates the clos- 
ing of this structure, and since an even older 
atrium exists below this one, Manchay Bajo 
must have been founded significantly before 
this time. Although most of the construction ep- 
isodes at Manchay Bajo date to the late Initial 



El Nino, Early Peruvian Civilization, and Human Agency 



95 




r 



Figure 2. Central mound at Manchay Bajo, Lurin Valley, during the 1998 excavations on the summit terraces. 
Modern agricultural constructions visible on the lower left are encroaching on the archaeological site. (Photograph 
by Richard L. Burger.) 



Period, the uppermost levels yielded a distinc- 
tive ceramic assemblage that dates to the Early 
Horizon; no hiatus is indicated (Fig. 4). The 
preliminary stylistic interpretation of the pot- 
tery is consistent with two AMS C14 measure- 
ments of 2560 50 B.P. (Beta- 122683) and 
2600 50 (AA 34441) from the final period 
of construction which, when calibrated, pro- 
duced a 2a range between 815-525 B.C. and 
894-539 B.C., respectively. Thus, the available 
evidence indicates that whereas Manchay Bajo 
was contemporary with Cardal and Mina Per- 
dida during the final centuries of the Initial Pe- 
riod, it continued to function as a civic-cere- 
monial center for a century or more after the 
others were abandoned (Fig. 5). Manchay Bajo 
is situated at the mouth of two quebradas that 
were incised into the Andean spur separating 
Lurin from the Rimac drainage (Fig. 6). The 
larger of these, known today as the Quebrada 
Manchay, is a dry tributary valley located to 
the north of Manchay Bajo. It is separated from 
the valley through which the Lurin River flows 
by a massive rocky spur (246 masl). The small- 



er of the two quebradas is located to the north- 
west of the site and is unnamed; it extends only 
for about a kilometer. The Quebrada Manchay 
was used as a natural corridor between the Lu- 
rin and Rimac in prehistoric times, and this 
route continues to be used today despite the 
poor state of the unpaved road. Given the nature 
of the topography and Manchay Bajo's location, 
a major El Nino could have triggered landslides 
through the large Quebrada Manchay, which 
would have buried the site's central plaza in 
stone rubble. A debris flow from the shorter, 
unnamed lateral quebrada would have had a 
strong effect on the western lateral platform of 
Manchay Bajo. Undeterred debris flows from 
either or both quebradas would have had the 
greatest impact on the residential zone covering 
the flatland to the north and northwest of the 
public architecture. 

The potential danger posed for prehistoric 
occupations and public spaces by landslides and 
debris flows from the small lateral quebrada 
was highlighted by the excavations at the site 
of Pampa Chica by archaeologists from the 



96 



R. L. Burger 




MAPA ARQUEOLOGICO 
MANCHAY BAJO 
PVA8_147 



Figure 3. Topographic map of the Manchay Bajo complex indicating the location of excavation units and the 
monumental wall extending along the western and northern extremes of the site. (Map drawn by Bernadino Ojeda.) 



Pontificia Universidad Catolica (PUC), Lima, 
under the direction of Jalh Dulanto as part of 
the Proyecto Arqueologico Tablada de Lurin, 
directed by Krzysztof Makowski. Pampa Chica, 



a small site located up the smaller of the two 
quebradas at 180 masl, had been covered by 
landslides. Occupied between the Early Hori- 
zon and the Middle Horizon, investigations at 



El Nino, Early Peruvian Civilization, and Human Agency 



97 




Figure 4. Incised fragment of a polished blackware vessel depicting a frontal face with two large fangs. This 
sherd from Manchay Bajo illustrates the pottery associated with the final phase of construction at the U-shaped 
pyramid complex. (Photograph by Richard L. Burger.) 



the site found evidence of repeated debris flows 
in prehistoric times (Dulanto et al. 2002). 

In addition to the danger posed to Manchay 
Bajo by flash floods and debris flows coming 
out of the Quebrada Manchay and the smaller 
lateral quebrada, a threat also was posed by a 
138-m-high rocky outcrop (278 masl) immedi- 
ately to the west of the main mound (Fig. 7). It 
is covered with large stone boulders and loose 
stone rubble, and this unconsolidated material 
would have become unstable during an El Nino 
event or an earthquake. 

Prior to 1998, no topographic map of the en- 
tire archaeological site of Manchay Bajo exist- 
ed. However, Harry Scheele (1970:179-190) 
had carried out test excavations at the site in 
1 966 and produced a sketch map of the central 



portion of the site. In subsequent years, many 
visitors, including Alberto Bueno Mendoza, 
members of the PUC Pampa Chicha team, and 
me, have examined Mancho Bajo and been in- 
trigued by a large wall that rings its western and 
northern perimeter. Our investigations included 
a detailed mapping of the entire site, and it was 
determined that the massive wall begins at a 
rocky outcrop near the southwest corner of the 
northwest lateral platform and runs in a north- 
erly direction for some 460 m. The wall then 
turns eastward and runs for another 240 m (see 
Fig. 3). Unfortunately, its final section was de- 
stroyed by the construction of a modern road, 
but it appears that the eastern end terminated 
45 m away, at the large rocky outcrop that de- 
fines the eastern edge of the Quebrada Man- 



98 



R. L. Burger 



700 



800 



900 



1000 



1100 



1200 



13CC 



Cardal 



Mina 
Perdida 



Manchay 
Bajo 



Figure 5. Radiocarbon measurements from the three U-shaped complexes excavated in the Lurin Valley dem- 
onstrate both the general contemporaneity of the centers and the continued occupation of Manchay Bajo after the 
abandonment of the other two sites. (Chart by George Lau.) 



chay. Both of the two extremes of the monu- 
mental wall appear to have been engaged with 
natural topographic features anchoring this re- 
markable cultural feature to the landscape. The 
total length of the original wall is estimated at 
745 m. 

During the mapping and surface survey in 
1998, masonry retaining walls could be seen at 
various points along both the north-south and 
east- west segments of the perimetric wall. In 
those sections where it has been exposed, the 
original wall can be seen to be double-faced, 
with a core of unconsolidated stone, gravel, and 
earth. In both segments there is evidence of at 
least one and in some cases two renovations of 
the wall; this was done by adding new walls 
separated from the previous walls by a layer of 
fill. These additions would have widened the 
wall substantially while reducing strain on the 
walls incorporated into the core. This same pat- 
tern of growth was determined for the terrace 
walls on the central pyramid of the Manchay 
Bajo complex. Like the Manchay Bajo's plat- 
form constructions, construction of the original 



monumental wall and its subsequent renovation 
were carried out with medium-sized blocks of 
roughly dressed stone from the nearby slopes 
(Fig. 8). Clay mortar was used at the junctures, 
but during the surface reconnaissance, no sur- 
viving evidence of surface plastering was en- 
countered. The width and height of the wall 
varied, and in many places its limits are com- 
pletely hidden under collapsed or accumulated 
material. Nevertheless, the topographic map 
suggested that the north-south segment had an 
average width of about 12.5 m and an average 
height of at least 5 m, and portions of the east- 
west segment were still more massive. Surface 
ceramics were encountered at various points on 
the summit of the wall; they were particularly 
common near its eastern end because of distur- 
bance from the modern construction of a small 
chapel on top of the wall. Based on vessel 
forms and decoration, all of the pottery can be 
dated to the late Initial Period. It included nu- 
merous shallow open bowls and neckless ollas. 
Some of the former had the vessel interior dec- 
orated with broad incisions. The surface ceram- 



El Nino, Early Peruvian Civilization, and Human Agency 



99 




Figure 6. Aerial photograph of Manchay Complex taken in 1945 displaying the relation of the pyramid complex 
to the two ravines or quebradas (on the viewer's left and upper left) and the Lurin River (on the viewer's right). The 
monumental wall can be seen anchored to two rocky outcrops to the west and north of the site. (Courtesy of Servicio 
Aereofotografico Nacional, Lima.) 



ics found on the wall in 1998 were indistin- 
guishable from those found in the excavations 
of the main mound at Manchay Bajo that same 
year. No later ceramics were on or near the 
wall. Based on the masonry style of the surface 
architecture and the ceramic evidence, a prelim- 
inary conclusion was reached that the monu- 
mental wall had been constructed during the 
Initial Period and was roughly contemporary 
with the adjacent U-shaped public architecture. 
Following the mapping and study of the 
monumental wall just described, we encoun- 
tered another masonry feature at the foot of the 
steep rocky outcrop to the west of the main pyr- 
amid (Fig. 9). Cut by a modern canal, ancient 
floors and fills were exposed, and these were 



reminiscent of features such as circular courts 
such as those found at Cardal. However, clear- 
ing and excavation in this area revealed that the 
remains actually corresponded to another mas- 
sive wall running for at least 105 m, with a 
width of 5 m and a height of 5 m. The stone- 
work and construction were similar to those al- 
ready described, and there was evidence of two 
episodes of renovation in which additional 
walls were added. In the 1 998 excavations of a 
small section of this wall, late Initial Period pot- 
tery was recovered from intact floor surfaces 
along the wall's eastern face. This evidence, 
combined with the construction style and tech- 
nique, lends support to the conclusion that this 
and the other monumental walls at Manchay 



100 



R. L. Burger 




Figure 7. Rocky outcrop immediately to the west of the Manchay Banjo complex. Traces of the monumental 
wall at the foot of the outcrop were visible prior to excavation and can be seen near the stadia rod in this 1998 
photograph. (Photograph by Richard L. Burger.) 



El Nino, Early Peruvian Civilization, and Human Agency 



101 




Figure 8. Excavation in 1999 of the eastern face of the monumental wall at Manchay Bajo. (Photograph by 
Richard L. Burger.) 



Bajo are coeval with the platform complex and 
were built by the same population. It is hypoth- 
esized that this wall was built to protect the area 
of the central mound from debris slides coming 
from the steep slopes of the rocky outcrop 
above it. Thus, the total extent of the monu- 
mental perimetric wall at Manchay Bajo must 
include this feature as well, bringing the total 
length of the wall constructions to some 850 m. 
If a rough calculation is made of the volume of 
earth and stone moved to construct these walls, 
it produces a figure in excess of 30,000 m 3 . 

In 1999, during the second field season, ar- 
chaeological excavations were carried out in a 
small section of the monumental wall (Sector 
VIIA, Excavation 3) in order to clarify its date, 
construction history, and the building tech- 
niques utilized. The work in this sector was su- 
pervised by Marcelo Saco (PUC), and technical 
assistance in the interpretation of the stratigra- 
phy was provided by the Polish sedimentolo- 
gist, Krzyzstof Mastalerz. The excavated units 
were located along the wall's north-south sec- 
tion, which crosses the mouth of the small lat- 
eral quebrada to the west of the site. Initially, 



7 m of the eastern face of the wall was cleared 
(see Fig. 8). This revealed that the southern half 
of this section was well-preserved, while the 
northern half had collapsed after the site's aban- 
donment. Subsequent excavations in the area 
focused on the intact portion of the wall; the 
zone investigated had an area of 49 m 2 . This 
included a 1-m-wide trench perpendicular to the 
wall face. At the conclusion of this excavation, 
a 17-m east- west transect of the monumental 
wall complemented the horizontal exposure of 
the wall's eastern face (Fig. 10). 

Judging from the excavations, the original 
monumental wall in this area was trapezoidal in 
cross-section. The hearting of the wall consists 
of loose soil, gravel, and stones. The wall was 
built on a sloping surface created by ephemeral 
sheet flows that predated the occupation of the 
site. Both faces of the wall consisted of roughly 
quarried medium-size stones (e.g., 40 X 38 cm) 
set in mud mortar. Both sides of the wall cant 
inward for greater stability, and as a result, the 
upper section of the wall is approximately 2 m 
in width and nearly 3 m wide at its base. The 
upper section of the original wall was missing. 



102 



R. L. Burger 




Figure 9. The clearing of the masonry visible at the foot of the western rocky outcrop revealed the eastern face 
of a monumental wall in association with Initial Period ceramics. Loose rock can be seen on the steep slopes above 
the wall. (Photograph by Richard L. Burger.) 



El Nino, Early Peruvian Civilization, and Human Agency 



103 




Figure 10. A trench transecting the monumental wall revealed the western face of the original monumental wall 
and evidence for two subsequent enlargements. The trowel rests upon a caliche-like layer formed as the result of 
floor deposits pooling up against the western face of the enlarged wall; this layer is absent on the interior or eastern 
side of the wall. (Photograph by Richard L. Burger.) 



104 



R. L. Burger 



It was feasible to reach the wall base on the 
western face, and it can be demonstrated that 
the original wall was over 2 m in height. 

Later in the history of Manchay Bajo, the 
wall was widened by stone retaining walls built 
parallel to the faces of the original wall. Along 
the eastern face the new retaining wall was ter- 
raced. The lower terrace was 1 m in height, and 
1.2 m remains of the upper terrace wall. Along 
the western face, sterile fills of gravel and stone 
were added, completely burying the original 
wall. The massive layers piled against the wall's 
original western face were studied in terms of 
their sorting and position, to determine whether 
they were man-made construction fills or the 
result of slumps or debris flows from the lateral 
quebrada. These layers include loose, frag- 
mented material ranging from angular boulders 
to muddy, coarse-grained sand. Sedimentologist 
K. Mastalerz (1999) concluded that they were 
man-made deposits piled against the western 
side of the original wall. These fills added at 
least 1 m in height and 4 m in width to the 
monumental wall, bringing the total scale of the 
wall in this section to over 9 m in width and 
over 3 m in height. 

Interestingly, the floor articulating with the 
western face of the original wall showed evi- 
dence of caliche-like cementation due to the 
precipitation of soluble compounds from 
groundwater. Mastalerz (1999) believes that 
such a layer was probably the result of the pool- 
ing of water from El Nino rains against the 
monumental wall. Significantly, this cementa- 
tion was not encountered along the eastern face 
of the wall. Little evidence survived of the new 
western face of the expanded monumental wall 
due to the narrowness of our trench (1m); only 
a limited portion of what remained could be 
exposed. However, the base of the wall (Muro 
6) and its associated floor was identified. Sur- 
prisingly, the wall was made of stone-filled shi- 
cra bags covered with mud mortar. This tech- 
nique of wall construction was rare at the 
U-shaped complexes in the Lurin Valley, but it 
had been identified previously at Mina Perdida 
(Burger and Salazar- Burger 2002). It was pos- 
sible to date the fiber used in the shicra in order 
to get an idea of the age of the monumental 
wall's renovation. The AMS measurement on 
this sample produced a date of 3020 40 B.P. 
(calibrated 2<r range of 1389-1129 B.C.). This 
result confirms the overall contemporaneity of 
the monumental wall with the U-shaped civic- 



ceremonial complex and the associated residen- 
tial constructions at Manchay Bajo. The date 
suggests that the original monumental wall was 
built early in the site's history and renovated at 
least once during the late Initial Period. Judging 
from the section excavated, that renovation may 
have involved as much labor as the original 
construction itself. Finally, it would appear 
from the caliche layer that a minimum of one 
major El Nino event occurred after the wall was 
constructed and while the site was still occu- 
pied. It is reasonable to hypothesize that this El 
Nino event may have stimulated the enlarge- 
ment of the original wall, since the addition 
covers the cementation. 

There are two other massive layers of gravel 
and stone that post-date Muro 6. According to 
Mastalerz, these, like the strata they cover, also 
are man-made deposits still in their original po- 
sition. A possible explanation of these strata is 
that they represent a subsequent second phase 
of enlargement after the collapse or dismantle- 
ment of the shicra wall (Muro 6). This enlarge- 
ment to the west could have involved a retain- 
ing wall whose traces have disappeared com- 
pletely, or, alternatively, as Mastalerz (1999) 
suggests, the final outer western surface of the 
monumental wall could have been left as an 
unfaced embankment. At the end of this hypo- 
thetical third construction phase, the monumen- 
tal wall would have reached 12 m in width and 
increased in height by at least another 50 cm to 
3.5 m. We have no way of directly dating this 
third episode of wall construction; we suspect 
that it could date to the final Early Horizon oc- 
cupation of the public center. 

The location of the walls, their massive 
width, and their substantial height all suggest 
that they were built as a dam to protect the civ- 
ic-ceremonial complex from land and rock 
slides coming off the rocky outcrops and out of 
the dry quebradas. It is significant that walls do 
not exist to the east or south of the Manchay 
Bajo complex, where there is no danger of such 
disasters. Moreover, there is evidence that the 
walls served their intended purpose with some 
success. In all four of the transects that we doc- 
umented in 1998, the surface level outside the 
wall (i.e., the exterior facing the potential 
source of debris) was significantly higher than 
inside the wall (i.e., the interior facing the plaza 
or platform mounds). It appears that in some 
areas, 1-2 m of material had accumulated 
against the wall, presumably from one or more 



El Nino, Early Peruvian Civilization, and Human Agency 



105 



debris flows provoked by El Ninos. In one deep 
cut to the north of the wall made by modern 
builders, this pattern of debris flow evidently 
recurred on several occasions both before and 
after the wall's construction. Judging from our 
excavations within the wall's perimeter, Man- 
chay Bajo's monumental wall or dam stopped 
the entry of stone rubble from debris flows, as 
was intended. In no area inside the wall did we 
encounter deposits of boulders or large stones 
carried by landslides or other disasters. The 
dam also appears to have protected the civic- 
ceremonial center from floods during the Initial 
Period and Early Horizon occupation of the 
site. 

Nevertheless, the problem posed by large 
quantities of flood water blocked by the mon- 
umental wall appears to have presented a seri- 
ous problem. Our investigations revealed that 
deep layers of water-borne deposits cover most 
of the site, with the exception of the elevated 
public architecture. For example, an excavation 
in the Manchay Bajo's open plaza area (Sector 
IV, Excavation 1) revealed that the central sec- 
tion of this space featured a low, stone-filled 
platform at least 1 m in height. This Initial Pe- 
riod construction was buried by over 2 m in 
flood deposits, which, according to Mastalerz 
(1999), were the product of six El Nino epi- 
sodes whose character varied in size and dura- 
tion. Some layers of sediments were the result 
of flash floods, while others were produced by 
powerful floods followed by stagnant water 
conditions. In one period the rains were suffi- 
cient to stimulate in-channel fluvial processes 
and the resulting deposition of sand and gravel 
bars at Manchay Bajo. The repeated floods doc- 
umented by these deposits came primarily from 
the Quebrada Manchay, and it would appear 
that the northern section of the dam was 
breached on numerous occasions during the last 
2000 years following the center's abandonment. 
Considerable numbers of Initial Period artifacts 
are mixed in with some of these flood deposits, 
and it is clear that these floods destroyed some 
of the upper layers of the site's Formative set- 
tlement. While there is compelling evidence of 
destructive floods following Manchay Bajo's 
abandonment, at the present time there is no 
evidence that floods disrupted the Initial Period 
or Early Horizon occupation of the civic-cere- 
monial center of Manchay Bajo. 



Agents and Environment 

The evidence summarized here suggests that ( 1 ) 
the people of Manchay Bajo perceived a threat 
to their center and adjacent agricultural lands 
from El Nino-related landslides; (2) they were 
able to generate a solution to the problem using 
available technology and materials; (3) they 
were able to mobilize enough labor to complete 
a dam large enough to protect them from El 
Nino debris slides; and (4) during some six cen- 
turies of occupation, they were able to bring 
together enough manpower to renovate the dam 
on at least two occasions by encasing the orig- 
inal wall within new fills and retaining walls. 
The monumental walls succeeded as bulwarks 
against the feared landslides, and they are still 
capable of doing so. These findings highlight 
the importance of human agency in shaping a 
culture's destiny; clearly, the actions discussed 
here were preemptive, anticipating potential 
threats from unpredictable future El Nino 
events. The population employed a knowledge 
of environmental risks to formulate a strategy, 
and they were able to implement this strategy 
even though it involved thousands of person- 
days of labor without immediate short-term 
benefit. 

The case of Manchay Bajo provides a good 
opportunity to reconsider some of our precon- 
ceptions about the ability of different kinds of 
societies to cope with environmental variability. 
It has often been assumed that states are 
uniquely well suited to deal with disasters be- 
cause of their coercive capacity, managerial ap- 
paratus, and ability to marshal resources from 
a wide area. Nevertheless, the continuity and 
duration of the Manchay culture for a millen- 
nium are a clear demonstration of the resilience 
and flexibility of its social forms in the face of 
mega-El Ninos and other disasters that must 
have occurred. In this respect, the Manchay cul- 
ture's lack of centralization and hierarchy may 
have been an asset rather than an obstacle. The 
mobilization of labor for efforts like the mon- 
umental wall should not surprise us, since even 
greater projects were undertaken during the sec- 
ond millennium to obtain water through gravity 
canals. In fact, the creation of new canals was 
intimately linked to the establishment of the ag- 
ricultural lands needed to support newly estab- 
lished social units and their public centers. Oth- 
er corporate labor efforts were undertaken to 



106 



R. L. Burger 



obtain supernatural favor through temple con- 
struction. 

The ability of the Manchay culture's subsis- 
tence economy to withstand short-term climatic 
disruptions is comprehensible, since its contin- 
ued dependence on a range of maritime resourc- 
es, hunting, and wild plants would have served 
the people well during an El Nino event. More- 
over, the social institutions underlying the im- 
pressive public constructions of the Manchay 
culture would have been an asset in times of 
crisis. In times of emergency, the annual mo- 
bilization of public labor usually used to refur- 
bish the U-shaped pyramid complexes could 
have been turned to repairing the relatively 
short canals that irrigated their fields and that 
would have been damaged by major El Nino 
events, or to renovate the monumental dam pro- 
tecting the site. 

As already noted, the construction technique, 
the masonry style, and the pattern of episodic 
renovations of the dam differ little from that 
used in the temple. In many respects, the chal- 
lenge of building a long linear feature like the 
Manchay Bajo dam is analogous to the con- 
struction of a gravity canal. Contemporary 
communities construct and maintain canals 
without state intervention by dividing the re- 
quired labor between the family units or com- 
munities that benefit from the irrigation water, 
with participation in the cooperative labor effort 
a prerequisite for continued community mem- 
bership (i.e., access to land and water). Such 
cooperative labor practices have been docu- 
mented for pre-Hispanic times, and may have 
been in place by the Initial Period (Burger 
1992; Mosely 1992). Considering these factors, 
it is worth considering whether the pre-state so- 
cieties of the Initial Period may have been as 
well as or, perhaps, even better equipped to deal 
with mega-El Niflos than the more fragile com- 
plex societies of later times. 

Acknowledgments. Research was conducted 
by permission of Peru's Institute Nacional de 
Cultura and made possible by grants from the 
Heinz Family Foundation, FERCO (the Foun- 
dation for Exploration and Research on Cultural 
Origins), and The Curtiss T. Brennan and Mary 
G. Brennan Foundation. I am deeply grateful to 
Lucy C. Salazar, Co-Director of the Proyecto 
Lurin, and to archaeologists Jose Pinilla, Ber- 
nadino Ojeda, and Marcel Savo, who helped to 
supervise the fieldwork. I am also indebted to 



Krzysztof Mastalerz for his insights into the 
sediments and depositional processes at Man- 
chay Bajo. 



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A Selected Listing of Other Andean Titles Available 



Useful Plants of the Siona and Secoya Indians of Eastern Ecuador. By William T. Vickers and Timothy 
Plowman. Fieldiana: Botany, n.s., no. 15, 1984. 63 pages, 24 illus. 

Publication 1356, $15.00 

The Ethnobotany of Chinchero, an Andean Community in Southern Peru. By Christine Franquemont et 
al. Fieldiana: Botany, n.s., no. 24, 1990. 126 pages, 34 illus., erratum. 

Publication 1408, $25.00 

Archaeological Research at Tumatumani, Juli, Peru. By Charles Stanish et al. Fieldiana: Anthropology, 
n.s., no. 23, 1993. Ill pages, 176 illus. 

Publication 1457, $23.00 

A Revision of the South American Species of Brunfelsia (Solanaceae). By Timothy Plowman. Edited 
posthumously by S. Knapp and J. R. Press. Fieldiana: Botany, n.s., no. 39, 1998. 135 pages, 46 illus. 
-i- 2 frontispieces (incl. a cool photograph of Tim). 

Publication 1496, $40.00 

The Early Ceramics of the Inca Heartland. By Brian S. Bauer. Fieldiana: Anthropology, n.s., no. 31, 
1999. 156 pages, 105 illus., 4 maps. 

Publication 1501, $60.00 

An Osteological Study of Nasca Trophy Heads Collected by A. L. Kroeber During the Marshall Field 
Expeditions to Peru. By Sloan R. Williams et al. Fieldiana: Anthropology, n.s., no. 33, 2001. 132 
pages, 84 illus. 

Publication 1516, $30.00 



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